original ) (raw )A rare subclinical or mild type of Becker muscular dystrophy caused by a single exon 48 deletion of the dystrophin gene
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Functional changes in Becker muscular dystrophy: implications for clinical trials in dystrophinopathies
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Journal of Biomedicine and Biotechnology, 2009
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Relatively low proportion of dystrophin gene deletions in Israeili Duchenne and Becker muscular dystrophy patients
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Amer J Med Genet, 1994
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Exon 46-48 Deletion of DMD Gene - A Boon in Beckers Muscular Dystrophy
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American Journal of Medical Genetics Part A, 2009
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Becker muscular dystrophy or spinal muscular atrophy?—Dystrophin studies resolve conflicting results of electromyography and muscle biopsy
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Causes of clinical variability in Duchenne and Becker muscular dystrophies and implications for exon skipping therapies
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Acta Myologica, 2020
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Deletion patterns of dystrophin gene in Hungarian patients with Duchenne/Becker muscular dystrophies
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Neuromuscular Disorders, 1999
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Patterns of dystrophin gene deletion in Egyptian Duchenne/Becker muscular dystrophy patients
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Saudi medical journal, 2002
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