Results 201 to 210 of about 75,574 (228)
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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
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, 1968H. Cohen, G. Molnar, L. T. Taft
semanticscholar +1 more source
Molecular studies of progressive muscular dystrophy (Duchenne).
Enzyme, 1987L. Kunkel +5 more
semanticscholar +1 more source
Dystrophin: The protein product of the duchenne muscular dystrophy locus
Cell, 1987Eric P. Hoffman +2 more
semanticscholar +1 more source
PSEUDOHYPERTROPHIC MUSCULAR DYSTROPHY: DUCHENNE TYPE.
Jornal de Pediatria, 1965R. Blattner
semanticscholar +1 more source
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
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, 2022Theodora Markati +5 more
semanticscholar +1 more source

