| Literature DB >> 1422198 |
D Rapaport1, M R Passos-Bueno, R I Takata, S Campiotto, S Eggers, M Vainzof, A Makover, U Nudel, D Yaffe, M Zatz.
Abstract
A total of 161 unrelated Duchenne (DMD) and Becker muscular dystrophy (BMD) patients were screened for deletions in the brain promoter region of the dystrophin gene. Southern blot analysis using a probe for the brain promoter detected a deletion in this region in only one of the DMD families, in a patient with normal intelligence. This deletion also included the promoter of the muscle-type dystrophin and the exons encoding the actin-binding and part of the spectrin-like domains. Our data suggest that deletions in the brain promoter region are rare in DMD and are compatible with normal intelligence.Entities:
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Year: 1992 PMID: 1422198 DOI: 10.1016/0960-8966(92)90043-6
Source DB: PubMed Journal: Neuromuscul Disord ISSN: 0960-8966 Impact factor: 4.296