The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.
about
A neonate with congenital amegakaryocytic thrombocytopenia associated with a chromosomal microdeletion at 21q22.11 including the gene RUNX1.Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population.Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study.
P2860
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.
description
2011 nî lūn-bûn
@nan
2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
name
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.
@ast
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.
@en
type
label
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.
@ast
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.
@en
prefLabel
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.
@ast
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.
@en
P2093
P2860
P50
P356
P1476
The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study
@en
P2093
Frederik H Aidt
Johanna C Moolman-Smook
Michael Christiansen
Ole Haundrup
P2860
P356
10.1186/1477-5751-10-12
P577
2011-10-03T00:00:00Z