Disease: Dyschromatosis symmetrica hereditaria 1
- A frameshift mutation in the ADAR gene in a Korean family with dyschromatosis symmetrica hereditaria
- A novel complex insertion-deletion mutation in ADAR1 gene in a Chinese family with dyschromatosis symmetrica hereditaria
- A novel deletion mutation of the ADAR1 gene in a Chinese patient with dyschromatosis symmetrica hereditaria
- A novel frameshift mutation of the ADAR1 gene in a Chinese patient with dyschromatosis symmetrica hereditaria and the dermoscopic features
- A novel insertion mutation in the ADAR1 gene of a Chinese family with dyschromatosis symmetrica hereditaria
- A novel missense mutation in ADAR1 gene causing dyschromatosis symmetrica hereditaria in a Chinese patient
- A novel missense mutation of ADAR1 gene in a Chinese family leading to dyschromatosis symmetrica hereditaria and literature review
- A novel mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria
- A novel mutation of the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria
- A novel nonsense mutation of ADAR1 gene in a Chinese patient with dyschromatosis symmetrica hereditaria
- A novel splice site mutation in the ADAR gene leading to exon skipping and dyschromatosis symmetrica hereditaria in a Japanese patient
- A-to-I RNA editing: a contribution to diversity of the transcriptome and an organism's development
- ADAR1 splicing mutation leading to dyschromatosis hereditaria in a Caucasian patient
- Analysis of a Chinese pedigree affected with dyschromatosis symmetrica hereditaria due to a novel variant of ADAR gene
- Analysis of ADAR gene mutations in two pedigrees affected with dyschromatosis symmetrica hereditaria
- Analysis of ADAR gene variant in a Chinese pedigree affected with dyschromatosis symmetrica hereditaria
- Analysis of ADAR gene variants in a Chinese pedigree affected with Dyschromatosis symmetrica hereditaria in conjunct with developmental delay
- Analysis of ADAR1 gene mutation in a pedigree affected with dyschromatosis symmetrical hereditaria
- Analysis of ADAR1 gene variants in two pedigrees affected with dyschromatosis symmetrica hereditaria
- Autosomal dominant ADAR c.3019G>A (p.(G1007R)) variant is an important mimic of hereditary spastic paraplegia and cerebral palsy
- Bilateral striatal necrosis and dyschromatosis symmetrica hereditaria: A-I editing efficiency of ADAR1 mutants and phenotype expression
- Case Report: Aicardi-Goutières Syndrome Type 6 and Dyschromatosis Symmetrica Hereditaria With Congenital Heart Disease and Mitral Valve Calcification - Phenotypic Variants Caused by Adenosine Deaminase Acting on the RNA 1 Gene Homozygous Mutations
- Co-occurrence of Aicardi-Goutières syndrome type 6 and dyschromatosis symmetrica hereditaria due to compound heterozygous pathogenic variants in ADAR1: a case series from India
- Conversion of röntgens to rads
- Decoupling expression and editing preferences of ADAR1 p150 and p110 isoforms
- Dermoscopic features in a case of dyschromatosis symmetrica hereditaria
- Detection of ADAR1 gene mutation in a family with dyschromatosis symmetrica hereditaria
- Differential Diagnosis of Two Chinese Families with Dyschromatoses by Targeted Gene Sequencing
- Diverse selective regimes shape genetic diversity at ADAR genes and at their coding targets
- Double-stranded RNA-specific adenosine deaminase (DSRAD) gene mutation in a Chinese family with dyschromatosis symmetrica hereditaria (DSH)
- Dowling-Degos disease
- Dyschromatosis symmetrica hereditaria
- Dyschromatosis Symmetrica Hereditaria and Aicardi-Goutières Syndrome 6 Are Phenotypic Variants Caused by ADAR1 Mutations
- Dyschromatosis symmetrica hereditaria and reticulate acropigmentation of Kitamura: An update
- Dyschromatosis symmetrica hereditaria associated with neurological disorders
- Dyschromatosis symmetrica hereditaria by ADAR1 mutations and viral encephalitis: a hidden link?
- Dyschromatosis symmetrica hereditaria complicated by intracranial hemangiomas and Parry-Romberg syndrome
- Dyschromatosis symmetrica hereditaria may be successfully controlled by topical sunscreen
- Dyschromatosis symmetrica hereditaria with acral hypertrophy
- Dyschromatosis symmetrica hereditaria with chilblains due to a novel two-amino-acid deletion in the double-stranded RNA-binding domain of ADAR1
- Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: report of a novel ADAR1 mutation
- Dyschromatosis symmetrica hereditaria with neurological abnormalities
- Dyschromatosis symmetrica hereditaria: a case report from Turkey, a new association and a novel gene mutation
- Dyschromatosis symmetrica hereditaria: A clue to early diagnosis of Aicardi-Goutières syndrome
- Dyschromatosis symmetrica hereditaria: report of a sporadic case
- Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23
- Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutation
- Eight Novel Mutations of the ADAR1 Gene in Chinese Patients with Dyschromatosis Symmetrica Hereditaria
- Eleven novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria
- First report of the coexistence of dyschromatosis symmetrica hereditaria and psoriasis: one novel TCT to A mutation in the double-RNA-specific adenosine deaminase gene
- Five novel mutations in the ADAR1 gene associated with dyschromatosis symmetrica hereditaria
- Five novel mutations of RNA-specific adenosine deaminase gene with dyschromatosis symmetrica hereditaria
- Four novel ADAR1 gene mutations in patients with dyschromatosis symmetrica hereditaria
- Four novel mutations of <em>ADAR1</em> in Chinese patients with dyschromatosis symmetrica hereditaria
- Four novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria
- Genetic analysis of a child with Dyschromatosis symmetrica hereditaria
- Genetic spectrum of dyschromatosis symmetrica hereditaria in Chinese patients including a novel nonstop mutation in ADAR1 gene
- Genetics of pigmentary disorders
- Genome-wide linkage and exome sequencing analyses identify an initiation codon mutation of KRT5 in a unique Chinese family with generalized Dowling-Degos disease
- Identification of a novel c.2633_2634del CT variant of the ADAR gene in a patient with dyschromatosis symmetrica hereditaria
- Identification of two novel splice mutations of the ADAR1 gene in two Chinese families with dyschromatosis symmetrica hereditaria
- Inherited Reticulate Pigmentary Disorders
- Investigation of the pathogenesis of ADAR1 gene in dyschromatosis symmetrica hereditaria
- Mendelian disease caused by variants affecting recognition of Z-DNA and Z-RNA by the Zα domain of the double-stranded RNA editing enzyme ADAR
- Multi-dimensional Insight into the Coexistence of Pathogenic Genes for ADAR1 and TSC2: Careful Consideration is Essential for Interpretation of ADAR1 Variants
- Mutation analyses of patients with dyschromatosis symmetrica hereditaria: five novel mutations of the ADAR1 gene
- Mutation analyses of patients with dyschromatosis symmetrica hereditaria: Ten novel mutations of the ADAR1 gene
- Mutation analysis of the ADAR1 gene in a Chinese Family with dyschromatosis symmetrica hereditaria
- Mutations in the ADAR1 gene in Chinese families with dyschromatosis symmetrica hereditaria
- Novel ADAR1 mutations in three cases of psoriasis coexisting with dyschromatosis symmetrica hereditaria
- Novel ADAR1 mutations including a single amino acid deletion in the deaminase domain underlie dyschromatosis symmetrica hereditaria in Japanese families
- Novel clinical and molecular findings in Chinese families with dyschromatosis symmetrica hereditaria
- Novel de novo heterozygous frameshift mutation of the ADAR1 gene in heavy dyschromatosis symmetrica hereditaria
- Novel mutations of the ADAR1 gene in two Chinese families with dyschromatosis symmetrica hereditaria
- Pathogenesis of a variant in the 5' untranslated region of ADAR1 in dyschromatosis symmetrica hereditaria
- Pathogenicity of ADAR1 mutation in a Chinese family with dyschromatosis symmetrica hereditaria
- Patient with dyschromatosis symmetrica hereditaria treated with miniature punch grafting, followed by excimer light therapy
- Recurrent Encephalopathy with Spinal Cord Involvement: An Atypical Manifestation of Aicardi-Goutières Syndrome
- Reticulate acropigmentation of dohi: a case report with insight into genodermatoses with mottled pigmentation
- Seven novel mutations of ADAR in multi-ethnic pedigrees with dyschromatosis symmetrica hereditaria in China
- Seven novel mutations of the ADAR gene in Chinese families and sporadic patients with dyschromatosis symmetrica hereditaria (DSH)
- Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: histological observation and comparison of genotypes and clinical phenotypes
- Study of 4 cases of total irradiation by radioactive cobalt (at respective doses of 250,400 and 600 rads) prior to an allogenic renal transplantation
- Sunlight is merely a temporary modifier of dyschromatosis symmetrica hereditaria
- Tables for the computation of the therapeutic absorption dose in rads in curietherapy of cancer of the cervix uteri
- Teaching surgery at the fel'dsher department of a medical school
- Ten novel mutations of the ADAR1 gene in Japanese patients with dyschromatosis symmetrica hereditaria
- The adenosine deaminase acting on RNA 1 p150 isoform is involved in the pathogenesis of dyschromatosis symmetrica hereditaria
- The c.3463C>T mutation of the ADAR1 gene in patients with dyschromatosis symmetrical hereditaria
- The role of RNA editing enzyme ADAR1 in human disease
- The spectrum of reticulate pigment disorders of the skin revisited
- Two frameshift mutations in the RNA-specific adenosine deaminase gene associated with dyschromatosis symmetrica hereditaria
- Two novel ADAR1 gene mutations in two patients with dyschromatosis symmetrical hereditaria from birth
- Two novel frameshift mutations of the DSRAD gene in Chinese pedigrees with dyschromatosis symmetrica hereditaria
- Two novel mutations in the DSRAD gene in two Chinese pedigrees with dyschromatosis symmetrica hereditaria
- Two novel mutations of the ADAR1 gene associated with dyschromatosis symmetrica hereditaria
- Two novel mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria
- Two novel mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria successfully treated with fractional CO2 laser
- Ultrastructural study of dyschromatosis symmetrica hereditaria with widespread pigmentary eruption
- What is the novel clinical finding in dyschromatosis symmetrica hereditaria?