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A novel exon 1 mutation in a patient with atypical lafora progressive myoclonus epilepsy seen as childhood-onset cognitive deficit
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Published in: | Epilepsia 2004, Vol.45 (3), p.294-295 |
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Main Authors: | , , , , , , , , , , , , , |
Format: | Report |
Language: | English |
Online Access: | Get full text |
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ISSN: | 0013-9580 |