Intranuclear Rod Myopathy

Known as: Intranuclear Nemaline Rod Myopathy, Nemaline Myopathy with Exclusively Intranuclear Rods 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2004-2017
0120042017

Papers overview

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2017
2017
Nemaline myopathy (NM) is a common form of congenital nondystrophic skeletal muscle disease characterized by muscular weakness of… (More)
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2016
2016
Actin plays a crucial role in regulating multiple processes within the nucleus, including transcription and chromatin… (More)
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2015
2015
Intranuclear rod myopathy (IRM), a variant of nemaline myopathy, is characterized by the presence of nemaline bodies in myonuclei… (More)
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2007
2007
Specific mutations within the alpha-skeletal actin gene (ACTA1) result in intranuclear rod myopathy (IRM), characterized by rod… (More)
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Review
2004
Review
2004
Congenital myopathies are clinical and genetic heterogeneous disorders characterized by skeletal muscle weakness ranging in… (More)
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