Amelioration of Muscle and Nerve Pathology in LAMA2 Muscular Dystrophy by AAV9-Mini-Agrin
Author:
Funder
NICHD
NIH/NINDS
Publisher
Elsevier BV
Subject
Genetics,Molecular Biology,Molecular Medicine
Reference49 articles.
1. Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin);Allamand;Eur. J. Hum. Genet.,2002
2. A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy;Pegoraro;Neurology,2000
3. Laminin alpha 2 (merosin)-deficient muscular dystrophy and demyelinating neuropathy in two cats;O’Brien;J. Neurol. Sci.,2001
4. Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models;Kuang;J. Clin. Invest.,1998
5. Genotype-phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations;Geranmayeh;Neuromuscul. Disord.,2010
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