Hereditary Hair Diseases (part 2)
Author:
Affiliation:
1. Department of Dermatology, Yamaguchi University Graduate School of Medicine
Publisher
Western Japan Division of JDA
Subject
Dermatology
Link
https://www.jstage.jst.go.jp/article/nishinihonhifu/80/3/80_239/_pdf
Reference42 articles.
1. 1) Shimomura Y, Christiano AM : Biology and genetics of hair. Annu Rev Genomics Hum Genet, 2010 ; 11 : 109-132.
2. 2) Kere J, Srivastava AK, Montonen O et al : X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein. Nat Genet, 1996 ; 13 : 409-416.
3. 3) Bayés M, Hartung AJ, Ezer S et al : The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats. Hum Mol Genet, 1998 ; 7 : 1661-1669.
4. 4) Monreal AW, Ferguson BM, Headon DJ, Street SL, Overbeek PA, Zonana J : Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nat Genet, 1999 ; 22 : 366-369.
5. 5) Headon DJ, Emmal SA, Ferguson BM et al : Gene defect in ectodermal dysplasia implicates a death domain adapter in development. Nature, 2001 ; 414 : 913-916.
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