The structure of the N-terminal actin-binding domain of human dystrophin and how mutations in this domain may cause Duchenne or Becker muscular dystrophy
Open Access
- 1 May 2000
- Vol. 8 (5) , 481-491
- https://doi.org/10.1016/s0969-2126(00)00132-5
Abstract
No abstract availableKeywords
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