A novel PIK3CD C896T mutation detected in bilateral sudden sensorineural hearing loss using next generation sequencing: An indication of primary immunodeficiency.
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A novel PIK3CD C896T mutation detected in bilateral sudden sensorineural hearing loss using next generation sequencing: An indication of primary immunodeficiency.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
A novel PIK3CD C896T mutation ...... n of primary immunodeficiency.
@en
A novel PIK3CD C896T mutation ...... n of primary immunodeficiency.
@nl
type
label
A novel PIK3CD C896T mutation ...... n of primary immunodeficiency.
@en
A novel PIK3CD C896T mutation ...... n of primary immunodeficiency.
@nl
prefLabel
A novel PIK3CD C896T mutation ...... n of primary immunodeficiency.
@en
A novel PIK3CD C896T mutation ...... n of primary immunodeficiency.
@nl
P2093
P2860
P1433
P1476
A novel PIK3CD C896T mutation ...... on of primary immunodeficiency
@en
P2093
Guiliang Zheng
Hongliang Zheng
Shiyue Chen
Xiangqiang Duan
P2860
P356
10.1016/J.JOTO.2016.06.001
P50
P577
2016-06-08T00:00:00Z