PRRT2 mutations in a cohort of Chinese families with paroxysmal kinesigenic dyskinesia and genotype-phenotype correlation reanalysis in literatures.
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PRRT2 mutations in a cohort of Chinese families with paroxysmal kinesigenic dyskinesia and genotype-phenotype correlation reanalysis in literatures.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年学术文章
@wuu
2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
@zh-sg
2017年學術文章
@yue
2017年學術文章
@zh
2017年學術文章
@zh-hant
name
PRRT2 mutations in a cohort of ...... ion reanalysis in literatures.
@en
PRRT2 mutations in a cohort of ...... ion reanalysis in literatures.
@nl
type
label
PRRT2 mutations in a cohort of ...... ion reanalysis in literatures.
@en
PRRT2 mutations in a cohort of ...... ion reanalysis in literatures.
@nl
prefLabel
PRRT2 mutations in a cohort of ...... ion reanalysis in literatures.
@en
PRRT2 mutations in a cohort of ...... ion reanalysis in literatures.
@nl
P2093
P2860
P1476
PRRT2 mutations in a cohort of ...... ion reanalysis in literatures.
@en
P2093
Guohua Zhao
Qiong Zhang
Xiaomin Liu
P2860
P356
10.1080/00207454.2017.1418345
P577
2017-12-29T00:00:00Z