Identification of a novelCOCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families-Reference-Cited by-同舟云学术

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Identification of a novelCOCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families

Published:2001 Issue:4 Volume:17 Page:351-351
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Kamarinos Maria,McGill Jim,Lynch Michael,Dahl Henrik

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 58 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. Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis;Biomolecules;2022-01-27

2. AudioGene: refining the natural history of KCNQ4, GSDME, WFS1, and COCH-associated hearing loss;Human Genetics;2022-01-17

3. On the pathophysiology of DFNA9: Effect of pathogenic variants in the COCH gene on inner ear functioning in human and transgenic mice;Hearing Research;2021-03

4. Inner Ear Proteins as Potential Biomarkers;Otology & Neurotology;2020-02

5. Cochlear involvement in patients with systemic autoimmune rheumatic diseases: a clinical and laboratory comparative study;European Archives of Oto-Rhino-Laryngology;2019-05-30

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