Modifier controls severity of a novel dominant low-frequency MyosinVIIA (MYO7A) auditory mutation-Reference-Cited by-同舟云学术

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Modifier controls severity of a novel dominant low-frequency MyosinVIIA (MYO7A) auditory mutation

Published:2004-05-01 Issue:5 Volume:41 Page:e62-e62
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Street V A

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 30 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. Monogenic Causes of Low-Frequency Non-Syndromic Hearing Loss;Audiology and Neurotology;2023

2. Clinical Heterogeneity Associated with MYO7A Variants Relies on Affected Domains;Biomedicines;2022-03-29

3. Clinical Profiles of DFNA11 at Diverse Stages of Development and Aging in a Large Family Identified by Linkage Analysis;Otology & Neurotology;2020-02-25

4. Development and Patterning of the Cochlea: From Convergent Extension to Planar Polarity;Cold Spring Harbor Perspectives in Medicine;2019-01-07

5. Identification of a MYO7A mutation in a large Chinese DFNA11 family and genotype–phenotype review for DFNA11;Acta Oto-Laryngologica;2018-02-05

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