Mutation-specific effects on thin filament length in thin filament myopathy.
about
Biallelic Mutations in MYPN, Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline MyopathyTropomodulins and Leiomodins: Actin Pointed End Caps and Nucleators in Muscles.Sarcomere Dysfunction in Nemaline Myopathy.Distortion of the Actin A-Triad Results in Contractile Disinhibition and Cardiomyopathy.Dysfunctional sarcomere contractility contributes to muscle weakness in ACTA1-related nemaline myopathy (NEM3).Sheep skeletal muscle transcriptome analysis reveals muscle growth regulatory lncRNAs.
P2860
Mutation-specific effects on thin filament length in thin filament myopathy.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 13 April 2016
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Mutation-specific effects on thin filament length in thin filament myopathy.
@en
Mutation-specific effects on thin filament length in thin filament myopathy.
@nl
type
label
Mutation-specific effects on thin filament length in thin filament myopathy.
@en
Mutation-specific effects on thin filament length in thin filament myopathy.
@nl
prefLabel
Mutation-specific effects on thin filament length in thin filament myopathy.
@en
Mutation-specific effects on thin filament length in thin filament myopathy.
@nl
P2093
P2860
P50
P356
P1433
P1476
Mutation-specific effects on thin filament length in thin filament myopathy.
@en
P2093
Barbara Joureau
C G Bönnemann
Carina Wallgren-Pettersson
Carol C Gregorio
Coen A C Ottenheijm
Edoardo Malfatti
Eun-Jeong Lee
Ger J M Stienen
Henk Granzier
Josine M de Winter
P2860
P304
P356
10.1002/ANA.24654
P50
P577
2016-04-13T00:00:00Z