A founder ectodysplasin A receptor (EDAR) mutation results in a high frequency of the autosomal recessive form of hypohidrotic ectodermal dysplasia in India-Reference-Cited by-同舟云学术

A founder ectodysplasin A receptor (EDAR) mutation results in a high frequency of the autosomal recessive form of hypohidrotic ectodermal dysplasia in India

Published:2012-03-05 Issue:4 Volume:166 Page:819-829
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:

Author:

Bashyam M.D.,Chaudhary A.K.,Reddy E.C.,Reddy V.,Acharya V.,Nagarajaram H.A.,Devi A.R.R.,Bashyam L.,Dalal A.B.,Gupta N.,Kabra M.,Agarwal M.,Phadke S.R.,Tainwala R.,Kumar R.,Hariharan S.V.

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2011.10707.x/fullpdf

Reference35 articles.

1. Mutations in EDAR account for one-quarter of non-ED1-related hypohidrotic ectodermal dysplasia;Chassaing;Hum Mutat,2006

2. Hypohidrotic (anhidrotic) ectodermal dysplasia: molecular genetic research and its clinical applications;Zonana;Semin Dermatol,1993

3. Ectodermal dysplasias: a clinical classification and a causal review;Pinheiro;Am J Med Genet,1994

4. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein;Kere;Nat Genet,1996

5. Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations;Monreal;Am J Hum Genet,1998

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