• A case of LSS-associated congenital nuclear cataract with hypotrichosis and literature review
• A Nonsense Variant in Hephaestin Like 1 (<em>HEPHL1</em>) Is Responsible for Congenital Hypotrichosis in Belted Galloway Cattle
• A novel heterozygous missense variant in ribosomal protein L21 associated with familial hypotrichosis simplex
• A novel homozygous mutation in <em>LSS</em> gene possibly causes hypotrichosis simplex in two siblings of a Tibetan family from the western Sichuan province of China
• A novel homozygous mutation in LSS gene possibly causes hypotrichosis simplex in two siblings of a Tibetan family from the western Sichuan province of China
• A Novel Pathogenic CDH3 Variant underlying Heredity Hypotrichosis Simplex detected by Whole-Exome Sequencing (WES)-A Case Report
• Additional causal SNRPE mutations in hereditary hypotrichosis simplex
• Alopecia areata and risk of common infections: a population-based cohort study
• Application of topical gentamicin-a new era in the treatment of genodermatosis
• Development of Woolly Hair and Hairlessness in a CRISPR-Engineered Mutant Mouse Model with KRT71 Mutations
• Diffuse congenital hypotrichosis simplex with associated hair shaft fragility
• Epidemiology, management and the associated burden of mental health illness, atopic and autoimmune conditions, and common infections in alopecia areata: protocol for an observational study series
• Familial hypotrichosis simplex of the scalp associated with a novel heterozygous nonsense variant in CDSN
• Four hypotrichosis families with mutations in the gene LSS presenting with and without neurodevelopmental phenotypes
• Genetic analysis of a child with Hypotrichosis simplex
• Hypotrichosis simplex of the scalp and peeling skin disease, two sides of the same coin
• Novel blended SNRPE-related spliceosomopathy phenotype characterized by microcephaly and congenital atrichia
• Successful treatment of hereditary hypotrichosis simplex by platelet rich plasma injection with topical minoxidil 2
• Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
• Two novel mutations in LSS gene associated with hypotrichosis simplex in a Chinese family