Behavioral characterization of mdx3cv mice deficient in C-terminal dystrophins
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference39 articles.
1. Dystrophin: the protein product of the Duchenne muscular dystrophy locus;Hoffman;Cell,1987
2. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patients;Nicholson;J Med Genet,1993
3. Cognitive functions in Duchenne muscular dystrophy: a reappraisal and comparison with spinal muscular atrophy;Billard;Neuromusc Disord,1992
4. Duchenne muscular dystrophy,1993
5. Duchenne muscular dystrophy gene product is not identical in muscle and brain;Nudel;Nature,1989
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