Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC.
about
A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8.Myofibrillar Myopathies: New Perspectives from Animal Models to Potential Therapeutic Approaches.HSPB7 prevents cardiac conduction system defect through maintaining intercalated disc integrity.FilaminA and Formin2 regulate skeletal, muscular, and intestinal formation through mesenchymal progenitor proliferation.A case report: a heterozygous deletion (2791_2805 del) in exon 18 of the filamin C gene causing filamin C-related myofibrillar myopathies in a Chinese family.
P2860
Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Cardiac arrhythmia and late-on ...... vel missense mutation in FLNC.
@en
type
label
Cardiac arrhythmia and late-on ...... vel missense mutation in FLNC.
@en
prefLabel
Cardiac arrhythmia and late-on ...... vel missense mutation in FLNC.
@en
P2093
P50
P1433
P1476
Cardiac arrhythmia and late-on ...... ovel missense mutation in FLNC
@en
P2093
D Avila-Smirnow
H-M Bécane
N B Romero
P304
P356
10.1016/J.NEUROL.2016.07.017
P577
2016-09-12T00:00:00Z