首页|期刊导航|中华耳科学杂志（英文版）|A novel PIK3CD C896T mutation detected in bilateral sudden sensorineural hearing loss using next generation sequencing:An indication of primary immunodeficiency
中华耳科学杂志（英文版）2016，Vol.11Issue(2)：78-83,6.DOI:10.1016/j.joto.2016.06.001
A novel PIK3CD C896T mutation detected in bilateral sudden sensorineural hearing loss using next generation sequencing:An indication of primary immunodeficiency
A novel PIK3CD C896T mutation detected in bilateral sudden sensorineural hearing loss using next generation sequencing:An indication of primary immunodeficiency
摘要
关键词
Sudden sensorineural hearing loss/Immunology/Genetics/Next generation sequencingKey words
Sudden sensorineural hearing loss/Immunology/Genetics/Next generation sequencing引用本文复制引用
Jing Zou,Xiangqiang Duan,Guiliang Zheng,Zhen Zhao,Shiyue Chen,Pu Dai,Hongliang Zheng..A novel PIK3CD C896T mutation detected in bilateral sudden sensorineural hearing loss using next generation sequencing:An indication of primary immunodeficiency[J].中华耳科学杂志（英文版）,2016,11(2):78-83,6.基金项目
This study was supported by the Ministry of Health Fund Industry of China, as part of project“Prevention, Intervention, and Extend Application of Deafness with Birth Defect”(contract #:201202005), and by the 1255 project of Changhai Hospital, Second Military Medical University, Shanghai, China （contract #:201202005）
