GJB2 (Connexin 26) mutations and childhood deafness in Thailand

GJB2 (Connexin 26) mutations and childhood deafness in Thailand

Hypothesis: The purpose of this study was to elucidate whether GJB2 mutations are responsible for childhood deafness in Southeast Asia. Background: GJB2 mutations are responsible for a large part of childhood deafness in many countries. In Whites, there is a common mutation (35delG) that accounts fo...

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Bibliographic Details
Main Authors: Takayuki Kudo, Katsuhisa Ikeda, Takeshi Oshima, Shigeo Kure, Maliwan Tammasaeng, Suchitra Prasansuk, Yoichi Matsubara
Other Authors: Tohoku University School of Medicine
Format: Article
Published: 2018
Subjects:
Medicine
Neuroscience
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/26892
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https://repository.li.mahidol.ac.th/handle/123456789/26892

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