Inclusion body myopathy, autosomal dominant

Known as: Inclusion body myopathy 3 
 
National Institutes of Health

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3 relations

Broader (3)

ContractureInclusion Body Myositis (disorder)Ophthalmoplegia

Papers overview

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2012
2012
Expression of the inclusion body myopathy 3 mutation in Drosophila depresses myosin function and stability and recapitulates muscle inclusions and weakness
Hereditary myosin myopathies are characterized by variable clinical features. Inclusion body myopathy 3 (IBM-3) is an autosomal… (More)
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