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. 1989 Jul 11;17(13):5391. doi: 10.1093/nar/17.13.5391

Two human cDNA molecules coding for the Duchenne muscular dystrophy (DMD) locus are highly homologous.

A Rosenthal ¹, A Speer ¹, H Billwitz ¹, G S Cross ¹, S M Forrest ¹, K E Davies ¹

PMCID: PMC318130 PMID: 2668885

5391

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Cross G. S., Speer A., Rosenthal A., Forrest S. M., Smith T. J., Edwards Y., Flint T., Hill D., Davies K. E. Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients. EMBO J. 1987 Nov;6(11):3277–3283. doi: 10.1002/j.1460-2075.1987.tb02646.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
Koenig M., Monaco A. P., Kunkel L. M. The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein. Cell. 1988 Apr 22;53(2):219–228. doi: 10.1016/0092-8674(88)90383-2. [DOI] [PubMed] [Google Scholar]
Rosenthal A., Speer A., Billwitz H., Cross G. S., Forrest S. M., Davies K. E. Nucleotide and corresponding amino acid sequence of human adult and fetal cDNA coding for portions of the Duchenne muscular dystrophy (DMD) gene. Biomed Biochim Acta. 1988;47(2):K13–K15. [PubMed] [Google Scholar]

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