Additional dystrophin fragment in Becker muscular dystrophy may result from proteolytic cleavage at deletion junctions
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference24 articles.
1. Dystrophin digest
2. Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide
3. Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy
4. A novel product of the Duchenne muscular dystrophy gene which greatly differs from the known isoforms in its structure and tissue distribution
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Pathological evaluation of rats carrying in-frame mutations in the dystrophin gene: A new model of Becker muscular dystrophy;Disease Models & Mechanisms;2020-01-01
2. Dystrophinopathies;Neuromuscular Disorders of Infancy, Childhood, and Adolescence;2015
3. Implications of a common polymorphism in intron 12 of the dystrophin gene for deletion detection by multiplex PCR;Gene;1998-03
4. Characterization of genetic deletions in becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophin;American Journal of Medical Genetics;1995-08-28
5. Is dystrophin always altered in Becker muscular dystrophy patients?;Journal of the Neurological Sciences;1995-07
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