Identification of novel variants in MYO15A, OTOF, and RDX with hearing loss by next‐generation sequencing

Identification of novel variants in MYO15A, OTOF, and RDX with hearing loss by next‐generation sequencing

Abstract Background Nonsyndromic hearing loss (NSHL) is the most common sensorineural disorder and one of the most common human defects. Autosomal recessive inheritance accounts for a huge percentage of familial cases. Next‐generation sequencing (NGS) is a powerful molecular diagnostic strategy for...

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Bibliographic Details
Main Authors: Xuejing Bai, Shiyan Nian, Lei Feng, Qingrong Ruan, Xuan Luo, Mengna Wu, Zefeng Yan
Format: Article
Language:English
Published: Wiley 2019-08-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
MYO15A
next‐generation sequencing
nonsyndromic hearing loss
OTOF
RDX
Online Access:https://doi.org/10.1002/mgg3.808

Internet

https://doi.org/10.1002/mgg3.808

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