有哪些信誉好的足球投注网站a duchenne muscular dystrophy gene hot spot mutation in dystrophin-deficient cavalier king charles spaniels is amenable to exon 51 skipping杜氏肌萎缩症基因热点突变在dystrophin-deficient骑士查理王猎犬是服从外显子51跳过.pdfVIP
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a duchenne muscular dystrophy gene hot spot mutation in dystrophin-deficient cavalier king charles spaniels is amenable to exon 51 skipping杜氏肌萎缩症基因热点突变在dystrophin-deficient骑士查理王猎犬是服从外显子51跳过
A Duchenne Muscular Dystrophy Gene Hot Spot
Mutation in Dystrophin-Deficient Cavalier King Charles
Spaniels Is Amenable to Exon 51 Skipping
1 2 1,2 3
Gemma L. Walmsley , Virginia Arechavala-Gomeza , Marta Fernandez-Fuente , Margaret M. Burke ,
4 5 1 1 6 2
Nicole Nagel , Angela Holder , Rachael Stanley , Kate Chandler , Stanley L. Marks , Francesco Muntoni ,
G. Diane Shelton7, Richard J. Piercy1,2*
1 Department of Veterinary Clinical Sciences, Royal Veterinary College, London, United Kingdom, 2 Dubowitz Neuromuscular Centre, Institute of Child Health, University
College London, United Kingdom, 3 Pathology Laboratory, Harefield Hospital, Royal Brompton Harefield NHS Foundation Trust, Harefield, Middlesex, United Kingdom,
4 Alphapet Veterinary Clinic, Bognor Regis, West Sussex, United Kingdom, 5 Pathology and Infectious Diseases, Royal Veterinary College, London, United Kingdom,
6 Department of Medicine Epidemiology, School of Veterinary Medicine, University of California Davis, Davis, California, United States of America, 7 Department of
Pathology, School of Medicine, University of California San Diego, La Jolla, California, United States of America
Abstract
Background: Duchenne muscular dystrophy (DMD), which afflicts 1 in 3500 boys, is one of the most common genetic
disorders of children. This fatal degenerative condition is caused by an absence or deficiency of dystrophin in striated
muscle. Most affected patients have inherited or spontaneous deletions in the dystrophin gene that disrupt the reading
fra
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