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. 1987 Dec 10;15(23):9761–9769. doi: 10.1093/nar/15.23.9761

Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the gene.

T J Smith 1, S M Forrest 1, G S Cross 1, K E Davies 1
PMCID: PMC306529  PMID: 3697082

Abstract

We have isolated overlapping human fetal muscle cDNAs encompassing 2.6kb which are localised very close to the 5' end of the Duchenne muscular dystrophy (DMD) gene. Using DNA from patients with deletions of previously reported genomic probes, we have mapped the exons across the region. Investigation of deletions in both DMD and Becker muscular dystrophy (BMD) patients shows the deletions to be present in 10% of cases and heterogeneous.

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Selected References

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

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