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Article

Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family.

International journal of pediatric otorhinolaryngology - 1 Apr 2016

Ma Yalin, Xiao Yun, Zhang Fengguo, Han Yuechen, Li Jianfeng, Xu Lei, Bai Xiaohui, Wang Haibo

Abstract excerpt

OBJECTIVES: Mutations in MYO7A gene have been reported to be associated with Usher Syndrome type 1B (USH1B) and nonsyndromic hearing loss (DFNB2, DFNA11). Most mutations in MYO7A gene caused USH1B, whereas only a few reported mutations led to DFNB2 and DFNA11. The current study was designed to investigate the mutations among a Chinese family with autosomal recessive hearing loss. METHODS: In this study, we...

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PMID: 26968074
DOI: 10.1016/j.ijporl.2016.01.001

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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