GJB2 (Connexin 26) mutations and childhood deafness in Thailand

• المؤلفون الرئيسيون: Takayuki Kudo, Katsuhisa Ikeda, Takeshi Oshima, Shigeo Kure, Maliwan Tammasaeng, Suchitra Prasansuk, Yoichi Matsubara
• مؤلفون آخرون: Tohoku University School of Medicine
• التنسيق: مقال
• منشور في: 2018
• الموضوعات: Medicine; Neuroscience
• الوصول للمادة أونلاين: https://repository.li.mahidol.ac.th/handle/123456789/26892
• المؤسسة: Mahidol University

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...