A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference15 articles.
1. A homozygous missense variant in type I keratin KRT25 causes autosomal recessive woolly hair;Ansar;J Med Genet,2015
2. A missense mutation within the helix initiation motif of the keratin K71 gene underlies autosomal dominant woolly hair/hypotrichosis;Fujimoto;J Invest Dermatol,2012
3. Development of a classification system for extrinsic hair damage: standard grading of electron microscopic findings of damaged hairs;Kim;Am J Dermatopathol,2010
4. Twelve-point scale grading system of scanning electron microscopic examination to investigate subtle changes in damaged hair surface;Lee;Skin Res Technol,2016
5. Correction of hair shaft defects through allele-specific silencing of mutant Krt75;Liu;J Invest Dermatol,2016
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