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2010 | 1 |
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Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease.
Epilepsia. 2010 Sep;51(9):1691-8. doi: 10.1111/j.1528-1167.2010.02692.x. Epub 2010 Aug 5.
Epilepsia. 2010.
PMID: 20738377
Free article.
Mutation spectrum and predicted function of laforin in Lafora's progressive myoclonus epilepsy.
Minassian BA, Ianzano L, Meloche M, Andermann E, Rouleau GA, Delgado-Escueta AV, Scherer SW.
Minassian BA, et al.
Neurology. 2000 Aug 8;55(3):341-6. doi: 10.1212/wnl.55.3.341.
Neurology. 2000.
PMID: 10932264
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