Human adhalin is alternatively spliced and the gene is located on chromosome 17q21.
Mutations in the dystrophin gene cause the X chromosome-linked, recessive Duchenne and Becker muscular dystrophies. Dystrophin, a large cytoskeletal protein, copurifies with a complex of dystrophin-associated proteins which serve to anchor dystrophin to the sarcolemma. One of these associated protei...
Zapisane w:
| Wydane w: | Proc Natl Acad Sci U S A |
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| Główni autorzy: | , , , , |
| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
National Academy of Sciences
1994
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC44882/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7937874/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.91.21.9690 |
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