Novel recessive myotilin mutation causes severe myofibrillar myopathy.
about
Single nucleotide variations: biological impact and theoretical interpretation.Dynamic transcriptome profiles of skeletal muscle tissue across 11 developmental stages for both Tongcheng and Yorkshire pigs.Mitochondrial abnormalities in the myofibrillar myopathies.Homozygosity of the Dominant Myotilin c.179C>T (p.Ser60Phe) Mutation Causes a More Severe and Proximal Muscular Dystrophy.
P2860
Novel recessive myotilin mutation causes severe myofibrillar myopathy.
description
2014 nî lūn-bûn
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2014 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունիսին հրատարակված գիտական հոդված
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2014年の論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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2014年論文
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2014年论文
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name
Novel recessive myotilin mutation causes severe myofibrillar myopathy.
@ast
Novel recessive myotilin mutation causes severe myofibrillar myopathy.
@en
type
label
Novel recessive myotilin mutation causes severe myofibrillar myopathy.
@ast
Novel recessive myotilin mutation causes severe myofibrillar myopathy.
@en
prefLabel
Novel recessive myotilin mutation causes severe myofibrillar myopathy.
@ast
Novel recessive myotilin mutation causes severe myofibrillar myopathy.
@en
P2093
P2860
P1433
P1476
Novel recessive myotilin mutation causes severe myofibrillar myopathy.
@en
P2093
Christiana Kubny
Elisa Bach
Franz-Georg Hanisch
Joachim Schessl
Sarah Feldkirchner
Simone Rost
Stefan Müller
Wolfram Kress
P2860
P2888
P304
P356
10.1007/S10048-014-0410-4
P577
2014-06-14T00:00:00Z