Identification of rare variants in TNNI3 with atrial fibrillation in a Chinese GeneID population
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Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery Disease.Identification of a mutation in CNNM4 by whole exome sequencing in an Amish family and functional link between CNNM4 and IQCB1.Genomic Variants in NEURL, GJA1 and CUX2 Significantly Increase Genetic Susceptibility to Atrial Fibrillation.De novo BK channel variant causes epilepsy by affecting voltage gating but not Ca2+ sensitivity.A loss-of-function mutation underlying familial atrial fibrillation
P2860
Identification of rare variants in TNNI3 with atrial fibrillation in a Chinese GeneID population
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh
2015年學術文章
@zh-hant
name
Identification of rare variant ...... in a Chinese GeneID population
@ast
Identification of rare variant ...... in a Chinese GeneID population
@en
type
label
Identification of rare variant ...... in a Chinese GeneID population
@ast
Identification of rare variant ...... in a Chinese GeneID population
@en
prefLabel
Identification of rare variant ...... in a Chinese GeneID population
@ast
Identification of rare variant ...... in a Chinese GeneID population
@en
P2093
P2860
P1476
Identification of rare variant ...... in a Chinese GeneID population
@en
P2093
Chengqi Xu
Chuchu Wang
Lisong Shi
Mian Cheng
Qing K Wang
Qiuyun Chen
P2860
P2888
P356
10.1007/S00438-015-1090-Y
P577
2015-07-14T00:00:00Z