bn:02360778n
Noun Concept
Categories: Articles containing potentially dated statements from 2004, Genetic disorders
EN
Desmin-related myofibrillar myopathy  myofibrillar myopathy 1  autosomal recessive limb-girdle muscular dystrophy type 2R  desmin-related myopathy  desminopathy
EN
Desmin-related myofibrillar myopathy, is a subgroup of the myofibrillar myopathy diseases and is the result of a mutation in the gene that codes for desmin which prevents it from forming protein filaments, instead forming aggregates of desmin and other proteins throughout the cell. Wikipedia
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EN
Desmin-related myofibrillar myopathy, is a subgroup of the myofibrillar myopathy diseases and is the result of a mutation in the gene that codes for desmin which prevents it from forming protein filaments, instead forming aggregates of desmin and other proteins throughout the cell. Wikipedia
Human disease Wikidata