| Literature DB >> 1822342 |
J T den Dunnen1, L Casula, A Makover, B Bakker, D Yaffe, U Nudel, G J van Ommen.
Abstract
Using a mouse genomic fragment containing the brain-specific promoter region of the dystrophin gene, we have located the brain promoter 75-300 kb proximal of the muscle promoter. Within our DMD-families we detected a patient who lacks both the brain-specific and muscle-specific promoter sequences. The normal intellectual capabilities of the patient argue against an indispensable role of the brain-specific first exon in mental functioning. The possibility exists that a NH2-terminally truncated dystrophin has taken over the function of the normal dystrophins in brain and/or muscle.Entities:
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Year: 1991 PMID: 1822342 DOI: 10.1016/0960-8966(91)90118-c
Source DB: PubMed Journal: Neuromuscul Disord ISSN: 0960-8966 Impact factor: 4.296