| Literature DB >> 8596935 |
L A Pennacchio1, A E Lehesjoki, N E Stone, V L Willour, K Virtaneva, J Miao, E D'Amato, L Ramirez, M Faham, M Koskiniemi, J A Warrington, R Norio, A de la Chapelle, D R Cox, R M Myers.
Abstract
Progressive myoclonus epilepsy of the Unverricht-Lundborg type (EPM1) is an autosomal recessive inherited form of epilepsy, previously linked to human chromosome 21q22.3. The gene encoding cystatin B was shown to be localized to this region, and levels of messenger RNA encoded by this gene were found to be decreased in cells from affected individuals. Two mutations, a 3' splice site mutation and a stop codon mutation, were identified in the gene encoding cystatin B in EPM1 patients but were not present in unaffected individuals. These results provide evidence that mutations in the gene encoding cystatin B are responsible for the primary defect in patients with EPM1.Entities:
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Year: 1996 PMID: 8596935 DOI: 10.1126/science.271.5256.1731
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728