Genotype-phenotype analysis of three Chinese families with Jervell and Lange-Nielsen syndrome.
about
A novel KCNQ1 nonsense variant in the isoform-specific first exon causes both jervell and Lange-Nielsen syndrome 1 and long QT syndrome 1: a case reportDigenic mutations on SCAP and AGXT2 predispose to premature myocardial infarction.Identification of KCNQ1 compound heterozygous mutations in three Chinese families with Jervell and Lange-Nielsen Syndrome.
P2860
Genotype-phenotype analysis of three Chinese families with Jervell and Lange-Nielsen syndrome.
description
2012 nî lūn-bûn
@nan
2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Genotype-phenotype analysis of ...... ll and Lange-Nielsen syndrome.
@ast
Genotype-phenotype analysis of ...... ll and Lange-Nielsen syndrome.
@en
type
label
Genotype-phenotype analysis of ...... ll and Lange-Nielsen syndrome.
@ast
Genotype-phenotype analysis of ...... ll and Lange-Nielsen syndrome.
@en
prefLabel
Genotype-phenotype analysis of ...... ll and Lange-Nielsen syndrome.
@ast
Genotype-phenotype analysis of ...... ll and Lange-Nielsen syndrome.
@en
P2093
P2860
P356
P1476
Genotype-phenotype analysis of ...... ll and Lange-Nielsen syndrome.
@en
P2093
Ruijuan Liang
Wenling Liu
Xiaoliang Qiu
Yuanfeng Gao
P2860
P356
10.4103/0975-3583.95357
P577
2012-04-01T00:00:00Z