Two novel ectodysplasin A gene mutations and prenatal diagnosis of X‐linked hypohidrotic ectodermal dysplasia-Reference-Cited by-同舟云学术

Two novel ectodysplasin A gene mutations and prenatal diagnosis of X‐linked hypohidrotic ectodermal dysplasia

Published:2021-09-28 Issue:11 Volume:9 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Yu Kang¹^ORCID,Shen Yihan¹,Jiang Cai‐Ling¹,Huang Wei²,Wang Feng²,Wu Yi‐Qun¹^ORCID

Affiliation:

1. Department of Second Dental Center Ninth People’s Hospital Affiliated with Shanghai Jiao Tong University School of Medicine Shanghai Key Laboratory of Stomatology National Clinical Research Center of Stomatology Shanghai China

2. Department of Oral Implantology Ninth People’s Hospital Affiliated with Shanghai Jiao Tong University School of Medicine Shanghai Key Laboratory of Stomatology National Clinical Research Center of Stomatology Shanghai China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1824

Reference32 articles.

1. The characterization of hypodontia, hypohidrosis, and hypotrichosis associated with X‐linked hypohidrotic ectodermal dysplasia: A systematic review

2. The Anhidrotic Ectodermal Dysplasia Gene (EDA) Undergoes Alternative Splicing and Encodes Ectodysplasin-A with Deletion Mutations in Collagenous Repeats

3. Hypohidrotic Ectodermal Dysplasia: A Multidisciplinary Approach

4. Prevalence and prevention of severe complications of hypohidrotic ectodermal dysplasia in infancy

5. Mutations inEDAR account for one-quarter of non-ED1-related hypohidrotic ectodermal dysplasia

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1. A Novel Ectodysplasin a Gene mutation of X-Linked Hypohidrotic Ectodermal Dysplasia;Clinical, Cosmetic and Investigational Dermatology;2024-06

2. Eight EDA mutations in Chinese patients with tooth agenesis and genotype–phenotype analysis;Oral Diseases;2024-01-29

3. Identification of six novel mutations in EDA from 20 hypohidrotic ectodermal dysplasia families;Oral Diseases;2023-12-21

4. Rare Pediatric Genetic Case Report of X-linked Hypohidrotic Ectodermal Dysplasia Type 1;Cureus;2023-12-02

5. Expanding the genetic spectrum of tooth agenesis using whole‐exome sequencing;Clinical Genetics;2022-09-17