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Showing articles 0 to 9 of 9 Filter Applied: dystrophin (Click to remove) Duchenne Muscular Dystrophy BMJ 368:L7012, Fox, H.,et al, 2020 Clinical Heterogeneity of Adhalin Deficiency Ann Neurol 39:196-202, Morandi,L.,et al, 1996 Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining Neurol 46:810-814, Connolly,A.M.,et al, 1996 Brief Report:Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy NEJM 329:921-925, 9601993., Muntoni,F.,et al, 1993 Cardiomyopathy May Be the Only Clinical Manifestation in Female Carriers of Duchenne Muscular Dystrophy Neurol 43:2342-2345, Mirabella,M.,et al, 1993 Dystrophinopathy in Isolated Cases of Myopathy in Females Neurol 42:967-975, Hoffman,E.P.,et al, 1992 Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989 Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene Neurol 39:1277-1280, Gospe,S.M.,et al, 1989 DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis Hum Genet 82:55-58, Defesche,J.C.,et al, 1989 Showing articles 0 to 9 of 9