dystrophin muscle protein domain terminal actin binding defects cause duchenne muscular dystrophy dmd |
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navigate by keyword : dystrophin cytoplasm muscle fiber costamere gene mutation sarcolemma myofiber myopathy muscular dystrophy duchenne duchene becker pdb1dxx actin binding cytoskeleton structure peptide protein amino acid molecule polypeptide polymer atoms science scientific disease health molecular model |
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Dystrophin muscle protein domain (N-terminal actin binding domain). Defects cause Duchenne muscular dystrophy (DMD). Cartoon representation combined with semi-transparent molecular surface |
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