• A case of Woodhouse-Sakati syndrome with pituitary iron deposition, cardiac and intestinal anomalies, with a novel mutation in DCAF17
• A diagnostic approach for neurodegeneration with brain iron accumulation: clinical features, genetics and brain imaging
• A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome
• A novel DCAF17 homozygous mutation in a girl with Woodhouse-Sakati syndrome and review of the current literature
• A novel splice site mutation in gene C2orf37 underlying Woodhouse-Sakati syndrome (WSS) in a consanguineous family of Pakistani origin
• A syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and ECG abnormalities
• Alopecia and hypotrichosis as characteristic findings in Woodhouse-Sakati syndrome: report of a family with mutation in the C2orf37 gene
• Brain MR Imaging Findings in Woodhouse-Sakati Syndrome
• C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients
• Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene
• Case Report: A Deletion Variant in the <em>DCAF17</em> Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
• Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
• Clinical Reasoning: Seven-year-old girl with progressive gait difficulties
• Corrigendum: Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene
• Deep Brain Stimulation in Rare Inherited Dystonias
• Dystonia in the Woodhouse Sakati syndrome: A new family and literature review
• Endocrine Abnormalities in a Case of Neurodegeneration with Brain Iron Accumulation
• Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
• Exome sequencing revealed a novel biallelic deletion in the DCAF17 gene underlying Woodhouse Sakati syndrome
• Expanding on the phenotypic spectrum of Woodhouse-Sakati syndrome due to founder pathogenic variant in DCAF17: Report of 58 additional patients from Qatar and literature review
• Genetic epidemiology of Woodhouse-Sakati Syndrome in the Greater Middle East region and beyond: a systematic review
• GENETICALLY DETERMINED DISEASES ASSOCIATED WITH PATHOLOGICAL BRAIN IRON ACCUMULATION AND NEURODEGENERATION
• Movement Disorders Associated with Hypogonadism
• Multimodal Evoked Potential Profiles in Woodhouse-Sakati Syndrome
• Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome
• Neurodegeneration with Brain Iron Accumulation Disorders Overview
• Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution
• Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse-Sakati syndrome
• Novel splicing-site mutation in DCAF17 gene causing Woodhouse-Sakati syndrome in a large consanguineous family
• Patterns of neurological manifestations in Woodhouse-Sakati Syndrome
• Phenotypic heterogeneity in Woodhouse-Sakati syndrome: two new families with a mutation in the C2orf37 gene
• Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
• Quantitative Susceptibility Mapping in Woodhouse-Sakati Syndrome
• Radiological Findings of Woodhouse-Sakati Syndrome: Cases Reported From Saudi Arabia
• The Successful Management of Primary Amenorrhea in Woodhouse-Sakati Syndrome: A Case Report and a Literature Review
• The syndrome of deafness-dystonia: clinical and genetic heterogeneity
• The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
• Three siblings with Woodhouse-Sakati syndrome in an Indian family
• Three Siblings With Woodhouse-Sakati Syndrome: A Case Report of A New Saudi Family
• Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse-Sakati syndrome
• Woodhouse and Sakati syndrome (MIM 241080): report of a new patient
• Woodhouse Sakati syndrome associated with bilateral keratoconus
• Woodhouse-Sakati Syndrome
• Woodhouse-Sakati syndrome (WSS): A case report of 3 Saudi sisters with urogenital anomalies
• Woodhouse-Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF17 gene
• Woodhouse-Sakati syndrome in an Indian patient with a novel pathogenic variant
• Woodhouse-Sakati syndrome in an Israeli-Arab family presenting with youth-onset diabetes mellitus and delayed puberty
• Woodhouse-Sakati Syndrome Presenting With Psychotic Features After Starting Trihexyphenidyl: A Case Report
• Woodhouse-Sakati syndrome: A review
• Woodhouse-Sakati syndrome: case report and symptoms review
• Woodhouse-Sakati Syndrome: First report of a Portuguese case
• Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation
• Woodhouse-Sakati Syndrome: The New Genetic Variant of DCAF17 In 2 Adult Sisters
• Writer's Cramp Presentation of Woodhouse-Sakati Syndrome - "Out of the Woods"