A novel PIK3CD C896T mutation detected in bilateral sudden sensorineural hearing loss using next generation sequencing:An indication of primary immunodeficiency

Jing Zou; Xiangqiang Duan; Guiliang Zheng; Zhen Zhao; Shiyue Chen; Pu Dai; Hongliang Zheng

doi:10.1016/j.joto.2016.06.001

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Home>Articles>A novel PIK3CD C896T mutation detected in bilateral sudden sensorineural hearing loss using next generation sequencing:An indication of primary immunodeficiency

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

Jing Zou

Xiangqiang Duan

Guiliang Zheng

Zhen Zhao

Shiyue Chen

Pu Dai

Hongliang Zheng

Keywords：Sudden sensorineural hearing lossImmunologyGeneticsNext generation sequencing

Publication Date：2016-01-01

Online Publishing Date：2025-08-15(First online date of this platform, not the publication date of the document)

Pages：6( 78-83 )

ISSN：1672-2930

Year, Vol.(Issue)：2016,11(2)