Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia-Reference-Cited by-同舟云学术

Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia

Published:2012-11 Issue:5 Volume:91 Page:906-911
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Lin Zhimiao,Chen Quan,Shi Lei,Lee Mingyang,Giehl Kathrin A.,Tang Zhanli,Wang Huijun,Zhang Jie,Yin Jinghua,Wu Lingshen,Xiao Ruo,Liu Xuanzhu,Dai Lanlan,Zhu Xuejun,Li Ruoyu,Betz Regina C.,Zhang Xue,Yang Yong

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference36 articles.

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2. Towards a unified classification of the ectodermal dysplasias: Opportunities outweigh challenges;Irvine;Am. J. Med. Genet. A.,2009

3. Pili torti and onychodysplasia. Report of a previously undescribed hidrotic ectodermal dysplasia;Calzavara-Pinton;Dermatologica,1991

4. A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type;Naeem;J. Med. Genet.,2006

5. Mutations in the keratin 85 (KRT85/hHb5) gene underlie pure hair and nail ectodermal dysplasia;Shimomura;J. Invest. Dermatol.,2010

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