GJB2 p.V37I Mutation Associated With Moderate Nonsyndromic Hearing Loss in an Adult Taiwanese Population.

doi:10.1097/AUD.0000000000001384

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Article

GJB2 p.V37I Mutation Associated With Moderate Nonsyndromic Hearing Loss in an Adult Taiwanese Population.

Ear and hearing - 1 Jan 2000

Yen Ting-Ting, Chen I-Chieh, Cho Sudi, Chang Ting-Gang, Shih Kai-Hsiang, Hua Men-Wei, Li Jui-Lin, Hsu Chiann-Yi, Hsiao Tzu-Hung, Chen Yi-Ming

Abstract excerpt

BACKGROUND: Gap junction protein beta 2 ( GJB2 ) p.V37I mutations are the most important hereditary cause of sensorineural hearing loss (SNHL) in Taiwan. Hearing outcomes are associated with hearing levels at baseline and the duration of follow-up. However, the audiological features of GJB2 p.V37I mutations in the adult population are unknown. The objectives of the present study were to investigate the...

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PMID: 37271870
DOI: 10.1097/AUD.0000000000001384

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