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- Title
Mutations in the MYO15A Gene Are a Significant Cause of Nonsyndromic Hearing Loss: Massively Parallel DNA Sequencing–Based Analysis.
- Authors
Miyagawa, Maiko; Nishio, Shin-ya; Hattori, Mitsuru; Moteki, Hideaki; Kobayashi, Yumiko; Sato, Hiroaki; Watanabe, Tomoo; Naito, Yasushi; Oshikawa, Chie; Usami, Shin-ichi
- Abstract
The article presents a study which concludes that the mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss based from the results of massively parallel DNA sequencing-based analysis. The materials and methods used in the study is described. The results and conclusions of the study are also provided.
- Subjects
COCHLEAR implants; GENES; HEARING disorders; JAPANESE people; GENETIC mutation; POLYMERASE chain reaction; RESEARCH funding
- Publication
Annals of Otology, Rhinology & Laryngology, 2015, Vol 124, p158S
- ISSN
0003-4894
- Publication type
Article
- DOI
10.1177/0003489415575058