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Ion channels in a skeletal muscle cell line from a Duchenne muscular dystrophy patient

✍ Scribed by Dr. Raul Caviedes; Dr. Pablo Caviedes; Dr. Jose L. Liberona; Dr. Enrique Jaimovich


Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
789 KB
Volume
17
Category
Article
ISSN
0148-639X

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For the first time in Bulgaria, a deletion/ duplication screening was performed on a group of 84 unrelated Duchennemecker muscular dystrophy patients, and the breakpoint distribution in the dystrophin gene was analyzed. Intragenic deletions were detected in 67.8% of patients, and intragenic duplicat