| Literature DB >> 3410474 |
S M Forrest1, G S Cross, T Flint, A Speer, K J Robson, K E Davies.
Abstract
Fetal muscle cDNA clones covering at least 11.4 kb of the Duchenne muscular dystrophy (DMD) gene sequence were used to identify a deletion-prone region in DNA from DMD and Becker muscular dystrophy (BMD) patients. Of 36 BMD cases, 17 (47%) had deletions and all of the deletions began in the same intron of the gene. Of 107 DMD patients, 27 (25%) were deleted for this region, and 19 deletions originate in the same intron. Using a cDNA probe for an adjacent region of the gene, 32 new deletions were detected in DMD patients (total 44%). No new BMD deletions were detected. The DMD deletions were very heterogeneous. Thus two cDNA probes covering 2.4 kb could detect 53% of these deletions. Considering the whole locus, DMD and BMD are caused by a deletion of the gene sequence in at least 67% of cases.Entities:
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Year: 1988 PMID: 3410474 DOI: 10.1016/0888-7543(88)90091-2
Source DB: PubMed Journal: Genomics ISSN: 0888-7543 Impact factor: 5.736