Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions-Reference-Cited by-同舟云学术

Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions

Published:2006-06 Issue:6 Volume:126 Page:1286-1291
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Schaffer Julie V.,Bazzi Hisham,Vitebsky Anna,Witkiewicz Agnieszka,Kovich Olympia I.,Kamino Hideko,Shapiro Lawrence S.,Amin Snehal P.,Orlow Seth J.,Christiano Angela M.

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference31 articles.

1. Desmoglein 4 is expressed in highly differentiated keratinocytes and trichocytes in human epidermis and hair follicle;Bazzi;Differentiation,2006

2. Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat;Bazzi;Differentiation,2004

3. C-cadherin ectodomain structure and implications for cell adhesion mechanisms;Boggon;Science,2002

4. Molecular abnormalities of the desmosomal protein desmoplakin in human disease;Cheong;Clin Exp Dermatol,2005

5. De novo mutations in monilethrix;Horev;Exp Dermatol,2003

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