https://pubmed.ncbi.nlm.nih.gov/3282674/
The complete sequence of the human Duchenne muscular dystrophy (DMD) cDNA has been determined. The 3685 encoded amino acids of the protein product, dystrophin,...
complete sequencea roddystrophinshapedcytoskeletal
https://pubmed.ncbi.nlm.nih.gov/12354438/
Mutations within the coding regions and splice junctions in the dystrophin gene only account for some cases of XLCM. Genetic heterogeneity and/or undetected...
comprehensivemutationscanningdystrophingene
https://pubmed.ncbi.nlm.nih.gov/24302611/
Duchenne muscular dystrophy (DMD) is associated with the loss of dystrophin, which plays an important role in myofiber integrity via interactions with...
zzdomaindystrophindmdmaking
https://pubmed.ncbi.nlm.nih.gov/12606026/
We analyzed dystrophin alternative splicing events in a large number of Becker muscular dystrophy (BMD) affected individuals presenting major hot-spot...
trans actingfactorsmaycausedystrophin
https://pubmed.ncbi.nlm.nih.gov/10932245/
Dystrophin and beta-dystroglycan are components of the dystrophin-glycoprotein complex (DGC), a multimolecular assembly that spans the cell membrane and links...
ww domainstructurecontainingfragmentdystrophin