A recurrent mutation in theAPCDD1gene responsible for hereditary hypotrichosis simplex in a large Chinese family
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2012.11001.x/fullpdf
Reference10 articles.
1. Congenital hair loss disorders: rare, but not too rare;Shimomura;J Dermatol,2012
2. Mutation in ribosomal protein L21 underlies hereditary hypotrichosis simplex;Zhou;Hum Mutat,2011
3. A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3;Betz;Am J Hum Genet,2000
4. Order and disorder in corneocyte adhesion;Ishida-Yamamoto;J Dermatol,2011
5. Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin;Levy-Nissenbaum;Nat Genet,2003
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2. Structure of WNT inhibitor adenomatosis polyposis coli down-regulated 1 (APCDD1), a cell-surface lipid-binding protein;Proceedings of the National Academy of Sciences;2023-05-08
3. Update of recent findings in genetic hair disorders;The Journal of Dermatology;2021-10-21
4. Disorders of Hair and Nails;Hurwitz Clinical Pediatric Dermatology;2016
5. Genetics of human isolated hereditary hair loss disorders;Clinical Genetics;2014-11-22
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