Glycoprotein-binding site of dystrophin is confined to the cysteine-rich domain and the first half of the carboxy-terminal domain
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(92)81265-N/fullpdf
Reference31 articles.
1. Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
2. Dystrophin: The protein product of the duchenne muscular dystrophy locus
3. The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein
4. Negative immunostaining of Duchenne muscular dystrophy(DMD) and mdx muscle surface membrane with antibody against synthetic peptide fragment predicted from DMD cDNA.
5. The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle
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