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Duchenne Muscular Dystrophy

2013
Duchenne muscular dystrophy (DMD) is the most common and severe form of muscular dystrophy and is caused by mutations in the dystrophin gene. Dystrophin, together with several other protein components, is part of a complex known as the dystrophin–glycoprotein complex (DGC).
J. Wicki, J.T. Seto, J.S. Chamberlain
openaire   +1 more source

The Genetic Relationship of Progressive Muscular Dystrophy (Duchenne Type) and Mental Retardation

Developmental Medicine & Child Neurology, 1968
H. Cohen, G. Molnar, L. T. Taft
semanticscholar   +1 more source

Molecular studies of progressive muscular dystrophy (Duchenne).

Enzyme, 1987
L. Kunkel   +5 more
semanticscholar   +1 more source

Dystrophin: The protein product of the duchenne muscular dystrophy locus

Cell, 1987
Eric P. Hoffman   +2 more
semanticscholar   +1 more source

Muscular Dystrophy, Duchenne

, 2014
Leslie D. Rosenstein
semanticscholar   +1 more source

Duchenne muscular dystrophy.

Current opinion in rheumatology, 1993
Advances in the understanding of the genetic basis for Duchenne muscular dystrophy over the past 4 years has led to the quick application of molecular diagnostics. More recently, attention has turned towards acquiring a better understanding of dystrophin biochemistry and the pathophysiologic consequences of dystrophin deficiency.
J R, Gorospe, E P, Hoffman
openaire   +1 more source

Emerging therapies for Duchenne muscular dystrophy

Lancet Neurology, 2022
Theodora Markati   +5 more
semanticscholar   +1 more source

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