| Literature DB >> 8476435 |
J P Hugnot1, H Gilgenkrantz, P Chafey, M Lambert, E Eveno, J C Kaplan, A Kahn.
Abstract
The dystrophin whose defect is responsible for Duchenne and Becker muscular dystrophies is present in muscle, brain and cerebellum. We describe here the detection of dystrophin in human cultured skin fibroblasts, L809 cells and murine 3T6 cell line. Dystrophin transcripts initiated at the muscle specific first exon can also be amplified by cDNA-PCR from various fibroblastic cells. The expression of the dystrophin gene in fibroblasts could account for some abnormalities observed in patient's fibroblast cultures.Entities:
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Year: 1993 PMID: 8476435 DOI: 10.1006/bbrc.1993.1382
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575