Five cases of paroxysmal kinesigenic dyskinesia by genetic diagnosis
about
A novel PRRT2 pathogenic variant in a family with Paroxysmal Kinesigenic Dyskinesia and Benign Familial Infantile Seizures.PRRT2 mutations in a cohort of Chinese families with paroxysmal kinesigenic dyskinesia and genotype-phenotype correlation reanalysis in literatures.Paroxysmal kinesigenic dyskinesia-like phenotype in multiple sclerosis.
P2860
Five cases of paroxysmal kinesigenic dyskinesia by genetic diagnosis
description
2014 nî lūn-bûn
@nan
2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Five cases of paroxysmal kinesigenic dyskinesia by genetic diagnosis
@ast
Five cases of paroxysmal kinesigenic dyskinesia by genetic diagnosis
@en
type
label
Five cases of paroxysmal kinesigenic dyskinesia by genetic diagnosis
@ast
Five cases of paroxysmal kinesigenic dyskinesia by genetic diagnosis
@en
prefLabel
Five cases of paroxysmal kinesigenic dyskinesia by genetic diagnosis
@ast
Five cases of paroxysmal kinesigenic dyskinesia by genetic diagnosis
@en
P2860
P356
P1476
Five cases of paroxysmal kinesigenic dyskinesia by genetic diagnosis
@en
P2093
Guo-Hong Chen
P2860
P304
P356
10.3892/ETM.2014.2155
P577
2014-12-22T00:00:00Z