Nemaline Myopathy, Autosomal Dominant

Known as: Autosomal Dominant Nemaline Myopathy 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1992-2007
01219922007

Papers overview

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2007
2007
The slow alpha-tropomyosin (TPM3) gene has to date been associated with few cases of both dominant and recessive nemaline… (More)
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2007
2007
We report a large family with a mild form of autosomal dominant nemaline myopathy and a new phenotype. Onset of symptoms was in… (More)
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2002
2002
We present a five-generation family with a novel phenotype of autosomal dominant nemaline myopathy not linked to the three genes… (More)
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2002
2002
We have previously reported a Met9Arg mutation in the human skeletal muscle alpha tropomyosin gene (TPM3) associated with… (More)
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1992
1992
Nemaline myopathy (NEM) is a neuromuscular disorder characterized by the presence, in skeletal muscle, of nemaline rods composed… (More)
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