Identification of four novel variants in the CDH23 gene from four affected families with hearing loss

Identification of four novel variants in the CDH23 gene from four affected families with hearing loss

Background: Hearing loss (HL) is the most common form of sensory disorder in humans. Molecular diagnosis of HL is important for genetic counseling for the affected individuals and their families.Methods: To identify potential genetic causes, we performed whole-exome sequencing and related biomedical...

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Bibliographic Details
Main Authors: Baoling Kang, Xinshu Lu, Jianjun Xiong, Yuan Li, Jinwen Zhu, Tao Cai
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-11-01
Series:Frontiers in Genetics
Subjects:
hearing loss
Cdh23
autosomal recessive
mutation
exome sequencing
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2022.1027396/full

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https://www.frontiersin.org/articles/10.3389/fgene.2022.1027396/full

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