Characterization of genetic deletions in becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophin
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference27 articles.
1. The frequency of patients with dystrophin abnormalities in a limb-girdle patient population
2. Additional dystrophin fragment in Becker muscular dystrophy may result from proteolytic cleavage at deletion junctions
3. Abnormal dystrophin expression in patients with limb girdle syndromes
4. An intact cysteine-rich domain is required for dystrophin function.
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2. From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies;Skeletal Muscle;2011
3. Monitoring Duchenne Muscular Dystrophy Gene Therapy with Epitope-Specific Monoclonal Antibodies;Methods in Molecular Biology;2010-12-08
4. Exon-specific dystrophin antibodies for studies of Duchenne muscular dystrophy;Translational Neuroscience;2010-01-01
5. A Rapid Method for Generating Large Numbers of High-Affinity Monoclonal Antibodies from a Single Mouse;Springer Protocols Handbooks;2009
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