about
Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function.Array lessons from the heart: focus on the genome and transcriptome of cardiomyopathies.Phospholamban C-terminal residues are critical determinants of the structure and function of the calcium ATPase regulatory complex.Familial hypertrophic cardiomyopathy: clinical features, molecular genetics and molecular genetic testing.Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings.
P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
name
Molecular diagnosis of myocardial disease.
@ast
Molecular diagnosis of myocardial disease.
@en
type
label
Molecular diagnosis of myocardial disease.
@ast
Molecular diagnosis of myocardial disease.
@en
prefLabel
Molecular diagnosis of myocardial disease.
@ast
Molecular diagnosis of myocardial disease.
@en
P2860
P356
P1476
Molecular diagnosis of myocardial disease.
@en
P2093
Neil E Bowles
P2860
P304
P356
10.1586/14737159.2.6.587
P577
2002-11-01T00:00:00Z