中华耳科学杂志（英文版）2016，Vol.11Issue(3)：134-137,4.
A screening analysis of the GJB2 c.176 del 16 mutation responsible for hereditary deafness in a Chinese family
A screening analysis of the GJB2 c.176 del 16 mutation responsible for hereditary deafness in a Chinese family
Hao Jiang 1Xi Shi 2Shiwei Qiu 2Yanfen Dong 2Yuehua Qiao 3Dongzhi Wei1
作者信息
- 1. New World Institute of Biotechnology, State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, 130 Meilong Road, 200237, Shanghai, China
- 2. The Institute of Audiology and Balance Science of Xuzhou Medical University, Xuzhou, 221004, China
- 3. Clinical Hearing Center of Affiliated Hospital of Xuzhou Medical University, Xuzhou, 221006, China
- 折叠
摘要
关键词
Deafness gene screening/GJB2/Gap junctionKey words
Deafness gene screening/GJB2/Gap junction引用本文复制引用
Hao Jiang,Xi Shi,Shiwei Qiu,Yanfen Dong,Yuehua Qiao,Dongzhi Wei..A screening analysis of the GJB2 c.176 del 16 mutation responsible for hereditary deafness in a Chinese family[J].中华耳科学杂志（英文版）,2016,11(3):134-137,4.
