Molecular Mechanisms and Clinical Phenotypes of <i>GJB2</i> Missense Variants

Molecular Mechanisms and Clinical Phenotypes of <i>GJB2</i> Missense Variants

The <i>GJB2</i> gene is the most common gene responsible for hearing loss (HL) worldwide, and missense variants are the most abundant type. <i>GJB2</i> pathogenic missense variants cause nonsyndromic HL (autosomal recessive and dominant) and syndromic HL combined with skin di...

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Bibliographic Details
Main Authors:	Lu Mao, Yueqiang Wang, Lei An, Beiping Zeng, Yanyan Wang, Dmitrij Frishman, Mengli Liu, Yanyu Chen, Wenxue Tang, Hongen Xu
Format:	Article
Language:	English
Published:	MDPI AG 2023-03-01
Series:	Biology
Subjects:	hereditary hearing loss <i>GJB2</i> missense variants molecular mechanisms deep mutational scanning
Online Access:	https://www.mdpi.com/2079-7737/12/4/505

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