Mutations in LOXHD1 gene cause various types and severities of hearing loss

OBJECTIVE: We present two families that were identified with novel mutations in LOXHD1, as a cause of non-progressive hearing loss. METHODS: One thousand three hundred fourteen (1,314) Japanese subjects with sensorineural hearing loss from unrelated families were enrolled in the study. Targeted geno...

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Publicado no:Ann Otol Rhinol Laryngol
Main Authors: Mori, Kentaro, Moteki, Hideaki, Kobayashi, Yumiko, Azaiez, Hela, Booth, Kevin T, Nishio, Shin-ya, Sato, Hiroaki, Smith, Richard J H, Usami, Shin-ichi
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4441841/
https://ncbi.nlm.nih.gov/pubmed/25792669
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0003489415574067
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