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Article

[Analysis of MYO15A variation in children with DFNB3].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 2 Oct 2020

Ren S M, Wu Q H, Jiao Z H, Chen Y B, Chen C, Kong X D, Qin Z B

Abstract excerpt

Objective: To analyze the genetic and clinical characteristics of MYO15A variants associated non-syndromic autosomal recessive deafness3 (DFNB3). Methods: The hearing test and high-throughput sequencing data of 108 families with non-syndromic hearing loss, who visited the Center of Genetics and Prenatal Diagnosis in the First Affiliated Hospital of Zhengzhou University from November 2016 to February 2019, were...

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PMID: 32987461
DOI: 10.3760/cma.j.cn112140-20200220-00115

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