A novel EDAR missense mutation identified by whole‐exome sequencing with non‐syndromic tooth agenesis in a Chinese family-Reference-Cited by-同舟云学术

A novel EDAR missense mutation identified by whole‐exome sequencing with non‐syndromic tooth agenesis in a Chinese family

Published:2021-05-04 Issue:6 Volume:9 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Zhang Hongyu¹,Kong Xuanting¹^ORCID,Ren Jiabao¹,Yuan Shuo¹,Liu Chunyan²,Hou Yan²,Liu Ye²,Meng Lingqiang¹,Zhang Guozhong³,Du Qingqing³,Shen Wenjing¹

Affiliation:

1. Department of Prosthodontics Hebei Key Laboratory of Stomatology Hebei Clinical Research Center for Oral Diseases School and Hospital of Stomatology Hebei Medical University Shijiazhuang PR China

2. Department of Orthodontics Hebei Key Laboratory of Stomatology Hebei Clinical Research Center for Oral Diseases School and Hospital of Stomatology Hebei Medical University Shijiazhuang PR China

3. College of Forensic Medicine Hebei Medical University Shijiazhuang PR China

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1684

Reference32 articles.

1. The novel EDAR p.L397H missense mutation causes autosomal dominant hypohidrotic ectodermal dysplasia

2. Candidate Gene Analysis of Tooth Agenesis Identifies Novel Mutations in Six Genes and Suggests Significant Role for WNT and EDA Signaling and Allele Combinations

3. Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases

4. Dental agenesis: genetic and clinical perspectives

5. Two EDA gene mutations in chinese patients with hypohidrotic ectodermal dysplasia

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