Arrhythmogenic inherited heart muscle diseases in children.
about
Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase.Cardiac features of a novel autosomal recessive dilated cardiomyopathic syndrome due to defective importation of mitochondrial protein.The CC genotype of the delta-sarcoglycan gene polymorphism rs13170573 is associated with obstructive sleep apnea in the Chinese population.The mutations associated with dilated cardiomyopathy
P2860
Arrhythmogenic inherited heart muscle diseases in children.
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Arrhythmogenic inherited heart muscle diseases in children.
@ast
Arrhythmogenic inherited heart muscle diseases in children.
@en
Arrhythmogenic inherited heart muscle diseases in children.
@nl
type
label
Arrhythmogenic inherited heart muscle diseases in children.
@ast
Arrhythmogenic inherited heart muscle diseases in children.
@en
Arrhythmogenic inherited heart muscle diseases in children.
@nl
prefLabel
Arrhythmogenic inherited heart muscle diseases in children.
@ast
Arrhythmogenic inherited heart muscle diseases in children.
@en
Arrhythmogenic inherited heart muscle diseases in children.
@nl
P356
P1476
Arrhythmogenic inherited heart muscle diseases in children.
@en
P2093
P304
P356
10.1054/JELC.2001.28859
P478
P577
2001-01-01T00:00:00Z