Thrombospondin-1 and disease progression in dysferlinopathy
Author:
Funder
Jain Foundation
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/26/24/4951/22854787/ddx378.pdf
Reference46 articles.
1. Redefining dysferlinopathy phenotypes based on clinical findings and muscle imaging studies;Neurology,2010
2. Clinical heterogeneity in dysferlinopathy;Intern. Med,2002
3. Making sense of the limb-girdle muscular dystrophies;Brain,1999
4. Dysferlin expression in monocytes: a source of mRNA for mutation analysis;Neuromuscul. Disord,2007
5. Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy;Nat. Genet,1998
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