Myogenesis in dysferlin-deficient myoblasts is inhibited by an intrinsic inflammatory response
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference49 articles.
1. Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy;Liu;Nat Genet,1998
2. Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations;Mahjneh;Neuromuscul Disord,2001
3. A gene for autosomal recessive limb-girdle muscular dystrophy maps to chromosome 2p;Bashir;Hum Mol Genet,1994
4. Making sense of the limb-girdle muscular dystrophies;Bushby;Brain,1999
5. Miyoshi-type distal muscular dystrophy. Clinical spectrum in 24 Dutch patients;Linssen;Brain,1997
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