A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family.
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A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family.
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2017 nî lūn-bûn
@nan
2017 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2017 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2017年の論文
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2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
name
A novel frameshift mutation of ...... ring loss in a Chinese family.
@ast
A novel frameshift mutation of ...... ring loss in a Chinese family.
@en
type
label
A novel frameshift mutation of ...... ring loss in a Chinese family.
@ast
A novel frameshift mutation of ...... ring loss in a Chinese family.
@en
prefLabel
A novel frameshift mutation of ...... ring loss in a Chinese family.
@ast
A novel frameshift mutation of ...... ring loss in a Chinese family.
@en
P2093
P2860
P50
P1433
P1476
A novel frameshift mutation of ...... ring loss in a Chinese family.
@en
P2093
Chufeng He
Hongsheng Chen
Juncheng Wang
Lingyun Mei
Xueping Wang
Xuezhong Liu
Yunpeng Dong
P2860
P304
P356
10.1371/JOURNAL.PONE.0178384
P407
P577
2017-05-25T00:00:00Z