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P1.1 Deletion of exon 26 of the dystrophin gene is associated with a mild Becker muscular dystrophy phenotype

✍ Scribed by N.W. Witting; M.D. Dunoe; J.V. Vissing


Book ID
116794943
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
61 KB
Volume
21
Category
Article
ISSN
0960-8966

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The DNA of a male harbored a deletion of exon 16 as well as most of introns 15 and 16 of the dystrophin gene. The person was completely healthy, with universal normal muscle strength, and normal muscle histology and creatine kinase levels. The deletion was also present in DNA from a muscle biopsy, e