about
Electrophysiological characteristics of R47W and A298T mutations in CLC-1 of myotonia congenita patients and evaluation of clinical features.Sequence CLCN1 and SCN4A in patients with Nondystrophic myotonias in Chinese populations: Genetic and pedigree analysis of 10 families and review of the literature.
P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Myotonia congenita: novel mutations in CLCN1 gene
@en
type
label
Myotonia congenita: novel mutations in CLCN1 gene
@en
prefLabel
Myotonia congenita: novel mutations in CLCN1 gene
@en
P2093
P2860
P1433
P1476
Myotonia congenita: novel mutations in CLCN1 gene
@en
P2093
Hai-Yan Zhou
Hui-Dong Tang
Jun-Yi Shen
Xiao-Jun Huang
Xiao-Li Liu
Xing-Hua Luan
P2860
P304
P356
10.1080/19336950.2015.1075676
P577
2015-08-11T00:00:00Z