Characterization of Lipid Binding Specificities of Dysferlin C2 Domains Reveals Novel Interactions with Phosphoinositides
Author:
Affiliation:
1. Neuromuscular Research Group, Montreal Neurological Institute and Hospital, McGill University, Montreal, Canada
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi802242r
Reference30 articles.
1. A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
2. Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
3. Distal anterior compartment myopathy: A dysferlin mutation causing a new muscular dystrophy phenotype
4. Defective membrane repair in dysferlin-deficient muscular dystrophy
5. Mutation impact on dysferlin inferred from database analysis and computer-based structural predictions
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