Dystrophin deficiency, altered cell signalling and fibre hypertrophy
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference98 articles.
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3. Familial X-linked myalgia and cramps: a non-progressive myopathy associated with a deletion in the dystrophin gene;Gospe;Neurology,1989
4. Becker muscular dystrophy: detection of unusual disease courses by combined approach to dystrophin analysis;Gold;Muscle Nerve,1992
5. Becker muscular dystrophy: an unusual presentation;Thakker;Arch Dis Child,1993
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