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Nemaline Myopathy, Autosomal Dominant

Known as: Autosomal Dominant Nemaline Myopathy 
National Institutes of Health

Related topics

Related topics

2 relations
Adult Onset Nemaline Myopathy

Broader (1)

Myopathies, Nemaline

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2007
2007
A second pedigree with autosomal dominant nemaline myopathy caused by TPM3 mutation: A clinical and pathological study
2007
2007
Autosomal dominant nemaline myopathy: A new phenotype unlinked to previously known genetic loci
2002
2002
A new phenotype of autosomal dominant nemaline myopathy
2002
2002
Expression and biological activity of Baculovirus generated wild-type human slow alpha tropomyosin and the Met9Arg mutant responsible for a dominant form of nemaline myopathy.
Highly Cited
1992
Highly Cited
1992
Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I.
Nemaline myopathy (NEM) is a neuromuscular disorder characterized by the presence, in skeletal muscle, of nemaline rods composed… 
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