Cardiomyopathies: classification, clinical characterization, and functional phenotypes.
about
Molecular mechanisms of cardiomyopathy phenotypes associated with myosin light chain mutationsTropomyosin is required for cardiac morphogenesis, myofibril assembly, and formation of adherens junctions in the developing mouse embryoNovel familial dilated cardiomyopathy mutation in MYL2 affects the structure and function of myosin regulatory light chain.
P2860
Cardiomyopathies: classification, clinical characterization, and functional phenotypes.
description
2012 nî lūn-bûn
@nan
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
2012年论文
@zh
2012年论文
@zh-cn
name
Cardiomyopathies: classification, clinical characterization, and functional phenotypes.
@en
Cardiomyopathies: classification, clinical characterization, and functional phenotypes.
@nl
type
label
Cardiomyopathies: classification, clinical characterization, and functional phenotypes.
@en
Cardiomyopathies: classification, clinical characterization, and functional phenotypes.
@nl
prefLabel
Cardiomyopathies: classification, clinical characterization, and functional phenotypes.
@en
Cardiomyopathies: classification, clinical characterization, and functional phenotypes.
@nl
P2093
P356
P1476
Cardiomyopathies: classification, clinical characterization, and functional phenotypes.
@en
P2093
Aldrin V Gomes
Danuta Szczesna-Cordary
Jeffrey R Moore
P304
P356
10.1155/2012/870942
P577
2012-12-04T00:00:00Z