Two EDA gene mutations in chinese patients with hypohidrotic ectodermal dysplasia-Reference-Cited by-同舟云学术

Two EDA gene mutations in chinese patients with hypohidrotic ectodermal dysplasia

Published:2018-03-06 Issue:8 Volume:32 Page:e324-e326
ISSN:0926-9959
Container-title:Journal of the European Academy of Dermatology and Venereology
language:en
Short-container-title:J Eur Acad Dermatol Venereol

Author:

Feng X.¹,Weng C.¹,Wei T.¹,Sun J.¹,Huang F.²,Yu P.¹,Qi M.¹³⁴⁵⁶

Affiliation:

1. Department of Cell Biology and Medical Genetics; School of Medicine; Zhejiang University; Hangzhou 310058 China

2. Department of Dermatology of Suxi Health-center; Yiwu 322009 China

3. Department of Pathology and Laboratory Medicine; University of Rochester; New York NY 14604 USA

4. Assisted Reproduction Unit; Department of Obstetrics and Gynecology; Sir Run Run Shaw Hospital; School of Medicine; Zhejiang University; Hangzhou 310016 China

5. Key Laboratory of Reproductive Dysfunction Management of Zhejiang Province; Hangzhou 310016 China

6. DIAN Diagnostics; Hangzhou 310024 China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Publisher

Wiley

Subject

Infectious Diseases,Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jdv.14874/fullpdf

Reference7 articles.

1. Clinical aspects of X-linked hypohidrotic ectodermal dysplasia;Clarke;Arch Dis Child,1987

2. Ectodermal dysplasia: retrospective study of fifteen cases;Yavuz;Arch Med Res,2006

3. Mutation screening of the Ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasia;Hout;Eur J Hum Genet,2008

4. Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases;Cluzeau;Hum Mutat,2011

5. A novel missense mutation in collagenous domain of EDA gene in a Chinese family with X-linked hypohidrotic ectodermal dysplasia;Li;J Genet,2015

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2. Ectodysplasin A/Ectodysplasin A Receptor System and Their Roles in Multiple Diseases;Frontiers in Physiology;2021-12-06

3. A novel EDAR missense mutation identified by whole‐exome sequencing with non‐syndromic tooth agenesis in a Chinese family;Molecular Genetics & Genomic Medicine;2021-05-04

4. Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR ‐ and EDA ‐associated nonsyndromic oligodontia;Human Mutation;2020-09-16

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