Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene-Reference-Cited by-同舟云学术

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Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene

Published:2000-01-31 Issue:1 Volume:106 Page:40-44
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Rabionet R.,Zelante L.,López-Bigas N.,D'Agruma L.,Melchionda S.,Restagno G.,Arbonés M.L.,Gasparini P.,Estivill X.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Cited by 192 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. Recent advances in genetic etiology of non-syndromic deafness in children;Frontiers in Neuroscience;2023-10-19

2. Gene Screening for Non-Syndromic Deafness in Hainanese Patients;The Journal of International Advanced Otology;2023-08-01

3. Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants;Biology;2023-03-27

4. Cochlear Implantation: The Volumetric Measurement of Vestibular Aqueduct and Gusher Prediction;Journal of Personalized Medicine;2023-01-19

5. Role of Connexin 43 phosphorylation on Serine-368 by PKC in cardiac function and disease;Frontiers in Cardiovascular Medicine;2023-01-12

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