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Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia.

Pubmed ID: 
25954030
Year: 
2015
Month: 
AUG
Volume: 
24
Issue: 
16
Citation: 
Damiano JA, Afawi Z, Bahlo M, Mauermann M, Misk A, Arsov T, Oliver KL, Dahl HH, Shearer AE, Smith RJ, Hall NE, Mahmood K, Leventer RJ, Scheffer IE, Muona M, Lehesjoki AE, Korczyn AD, Herrmann H, Berkovic SF, Hildebrand MS. Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia. HUMAN MOLECULAR GENETICS 24 (16) : 4483 - 90(2015) PubMed (Grant IDs: 628952, 466671, 1006110, 1063799, APP1054618)