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Neurology|July 27, 2005
New calcium channel mutations predict aberrant RNA splicing in episodic ataxiaLouise H Eunson, Tracey D Graves, Michael G HannaThe Journal of Physiology|January 5, 2002
Variable K(+) channel subunit dysfunction in inherited mutations of KCNA1Ruth Rea, Alexander Spauschus, Louise H Eunson, et al.Brain : a Journal of Neurology|October 16, 2004
Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxiaPaola Imbrici, Stephen L Jaffe, Louise H Eunson, et al.Neurobiology of Disease|July 9, 2008
Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2Tracey D Graves, Paola Imbrici, Esther E Kors, et al.Brain : a Journal of Neurology|November 8, 2005
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic dataNaheed L Khan, Shushant Jain, John M Lynch, et al.Pageof 1