X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein-Reference-Cited by-同舟云学术

X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

Published:1996-08 Issue:4 Volume:13 Page:409-416
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Kere Juha,Srivastava Anand K.,Montonen Outi,Zonana Jonathan,Thomas Nick,Ferguson Betsy,Munoz Felix,Morgan Delyth,Clarke Angus,Baybayan Primo,Chen Ellson Y.,Ezer Sini,Saarialho-Kere Ulpu,de la Chapelle Albert,Schlessinger David

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0896-409.pdf

Reference46 articles.

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2. McKusick, V.A., Mendelian in heritance in Man. 11th edn. (Johns Hopkins University Press, Baltimore, 1994).

3. Freire-Maia, N. & Pinheiro, M. Ectodermal dysplasias: a clinical and genetic study. (Alan R. Liss, New York, 1984).

4. Freire-Maia, N. & Pinheiro, M. Ectodermal dysplasias: a clinical classification and a causal review. Am. J. Med. Genet. 53, 153–162 (1994).

5. Reed, W.B., Lopez, D.A. & Landing, B. Clinical spectrum of anhidrotic ectodermal dysplasia. Arch. Derm. 102, 134–143 (1970).

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