From ectodermal dysplasia to selective tooth agenesis
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32801/fullpdf
Reference18 articles.
1. The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats;Bayés;Hum Mol Genet,1998
2. Mutations in EDAR account for one-quarter of non-ED1-related hypohidrotic ectodermal dysplasia;Chassaing;Hum Mut,2006
3. Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein;Elomaa;Hum Mol Genet,2001
4. Mutations in the EDA gene are responsible for X-linked hypohidrotic ectodermal dysplasia and hypodontia in Chinese kindreds;Fan;Eur J Oral Sci,2008
5. Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis;Han;Eur J Med Genet,2008
Cited by 23 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Identification of novel candidate genes associated with non-syndromic tooth agenesis in Mongolian families;Clinical Oral Investigations;2023-12-29
2. New observation of severe tooth malformation in a female patient with ectodermal dysplasia due to the EDA splice acceptor variant c.742‐2A>G;Molecular Genetics & Genomic Medicine;2023-09-04
3. Identification of novel candidate genes associated with non-syndromic tooth agenesis in Mongolian families;2023-05-02
4. The EDA/EDAR/NF-κB pathway in non-syndromic tooth agenesis: A genetic perspective;Frontiers in Genetics;2023-04-03
5. Common variants of EDA are associated with non‐syndromic hypodontia;Orthodontics & Craniofacial Research;2020-09-07
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