A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews-Reference-Cited by-同舟云学术

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A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews

Published:2001 Issue:5 Volume:18 Page:460-460
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Lerer Israela,Sagi Michal,Ben-Neriah Ziva,Wang Tieling,Levi Haya,Abeliovich Dvorah

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 185 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

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2. Explanations for the discrepancy between variant frequency and homozygous disease occurrence: Lessons from Ashkenazi Jewish data;European Journal of Medical Genetics;2023-06

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4. Cx26 heterozygous mutations cause hyperacusis-like hearing oversensitivity and increase susceptibility to noise;Science Advances;2023-02-10

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