| Literature DB >> 8469976 |
Y H Fu1, D L Friedman, S Richards, J A Pearlman, R A Gibbs, A Pizzuti, T Ashizawa, M B Perryman, G Scarlato, R G Fenwick.
Abstract
The myotonic dystrophy mutation has recently been identified; however, the molecular mechanism of the disease is still unknown. The sequence of the myotonin-protein kinase gene was determined, and messenger RNA spliced forms were identified in various tissues. Antisera were developed for analytical studies. Quantitative reverse transcription-polymerase chain reaction and radioimmunoassay were used to demonstrate that decreased levels of the messenger RNA and protein expression are associated with the adult form of myotonic dystrophy.Entities:
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Year: 1993 PMID: 8469976 DOI: 10.1126/science.8469976
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728