Congenital myopathy caused by a novel missense mutation in the CFL2 gene.
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Approach to the diagnosis of congenital myopathiesPathophysiological concepts in the congenital myopathies: blurring the boundaries, sharpening the focusCofilin-2 controls actin filament length in muscle sarcomeres.Skeletal muscle microRNA and messenger RNA profiling in cofilin-2 deficient mice reveals cell cycle dysregulation hindering muscle regeneration.Clinical utility gene card for: Nemaline myopathy - update 2015.A two-segment model for thin filament architecture in skeletal muscle.Biophysics of actin filament severing by cofilinSarcomere Dysfunction in Nemaline Myopathy.Novel functions for ADF/cofilin in excitatory synapses - lessons from gene-targeted miceOverview of the Muscle Cytoskeleton.Molecular Genetics of Nemaline Myopathy
P2860
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P2860
Congenital myopathy caused by a novel missense mutation in the CFL2 gene.
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
Congenital myopathy caused by a novel missense mutation in the CFL2 gene.
@ast
Congenital myopathy caused by a novel missense mutation in the CFL2 gene.
@en
type
label
Congenital myopathy caused by a novel missense mutation in the CFL2 gene.
@ast
Congenital myopathy caused by a novel missense mutation in the CFL2 gene.
@en
prefLabel
Congenital myopathy caused by a novel missense mutation in the CFL2 gene.
@ast
Congenital myopathy caused by a novel missense mutation in the CFL2 gene.
@en
P2093
P2860
P50
P1476
Congenital myopathy caused by a novel missense mutation in the CFL2 gene
@en
P2093
A Dara Hama-Amin
A Diekstra
E J Kamsteeg
H J Gilhuis
N V A M Knoers
N van Alfen
P B Agrawal
P2860
P304
P356
10.1016/J.NMD.2012.03.008
P577
2012-05-04T00:00:00Z