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Familial cortical myoclonic tremor and epilepsy (FCMTE): Refinement of the fcmte2 locus and confirmation of a founder haplotype

✍ Scribed by Licchetta, L.; Pippucci, T.; Bisulli, F.; Cantalupo, G.; Alvisi, L.; Martinelli, P.; Naldi, I.; Liguori, R.; Zara, F.; Seri, M.; Tinuper, P.


Book ID
121768444
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
60 KB
Volume
333
Category
Article
ISSN
0022-510X

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## Abstract Fifty Japanese and European families with cortical myoclonic tremor and epilepsy have been reported under various names. Unfamiliarity with the syndrome often leads to an initial misdiagnosis of essential tremor or progressive myoclonus epilepsy. A detailed overview of the literature is