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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

✍ Scribed by Fiona LM Norwood; Andrew J Sutherland-Smith; Nicholas H Keep; John Kendrick-Jones


Book ID
114328708
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
804 KB
Volume
8
Category
Article
ISSN
0969-2126

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