Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation.
about
Desminopathies in muscle disease.Desminopathies: pathology and mechanisms.Viral-mediated expression of desmin mutants to create mouse models of myofibrillar myopathy.Intermediate filaments: primary determinants of cell architecture and plasticity.Desmin-related myopathy.On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria.Proteasomal expression, induction of immunoproteasome subunits, and local MHC class I presentation in myofibrillar myopathy and inclusion body myositis.Actin-related myopathy without any missense mutation in the ACTA1 gene.Molecular insights into cardiomyopathies associated with desmin (DES) mutations
P2860
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P2860
Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation.
description
2000 nî lūn-bûn
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2000年の論文
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2000年学术文章
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name
Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation.
@en
Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation.
@nl
type
label
Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation.
@en
Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation.
@nl
prefLabel
Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation.
@en
Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation.
@nl
P2093
P2860
P1433
P1476
Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutation.
@en
P2093
Dalakas MC
Ferrans VJ
Goldfarb LG
Semino-Mora C
P2860
P304
P356
10.1034/J.1399-0004.2000.570604.X
P577
2000-06-01T00:00:00Z