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Article

Mutations in the MYO15A Gene Are a Significant Cause of Nonsyndromic Hearing Loss

19 Mar 2015

Abstract excerpt

OBJECTIVES: Screening for MYO15A mutations was carried out using a large cohort to clarify the frequency and clinical characteristics of patients with MYO15A (DFNB3) mutations in a hearing loss population. METHODS: Genetic analysis of 63 previously reported deafness genes based on massively parallel DNA sequencing (MPS) in 1120 Japanese hearing loss patients from 53 otorhinolaryngology departments was performed....

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PMID: 25792667
DOI: 10.1177/0003489415575058

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Mutations in the MYO15A Gene Are a Significant Cause of Nonsyndromic Hearing LossPMID 25792667Read ↗

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