Some unanswered questions in Duchenne muscular dystrophy
- 31 July 1994
- journal article
- editorial
- Published by Elsevier in Neuromuscular Disorders
- Vol. 4 (4) , 301-303
- https://doi.org/10.1016/0960-8966(94)90065-5
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Factor VIII gene rearrangements in patients with severe haemophilia AThe Lancet, 1994
- Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated CardiomyopathyNew England Journal of Medicine, 1993
- Progress in Defining the Causes of Idiopathic Dilated CardiomyopathyNew England Journal of Medicine, 1993
- Two distinct mutations in a single dystrophin gene: Identification of an altered splice‐site as the primary becker muscular dystrophy mutationAmerican Journal of Medical Genetics, 1993
- X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.Circulation, 1993
- An alternative dystrophin transcript specific to peripheral nerveNature Genetics, 1993
- Functional significance of dystrophin positive fibres in Duchenne muscular dystrophy.Archives of Disease in Childhood, 1993
- The structural and functional diversity of dystrophinNature Genetics, 1993
- The cardiomyopathy of Duchenne's muscular dystrophy and the function of dystrophinMedical Hypotheses, 1993
- Two hot spots of recombination in the DMD gene correlate with the deletion prone regionsHuman Molecular Genetics, 1992