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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 10, 2024. (Total: 232398Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Seizures and CACNA1H[original query]
Gating effects of mutations in the Cav3.2 T-type calcium channel associated with childhood absence epilepsy.
The Journal of biological chemistry 2004 1 279 (11): 9681-4.
Khosravani Houman, Altier Christophe, Simms Brett, Hamming Kevin S, Snutch Terrance P, Mezeyova Janette, McRory John E, Zamponi Gerald
Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants.
Annals of neurology 2007 Dec 62 (6): 560-8.
Heron Sarah E, Khosravani Houman, Varela Diego, Bladen Chris, Williams Tristiana C, Newman Michelle R, Scheffer Ingrid E, Berkovic Samuel F, Mulley John C, Zamponi Gerald
Clinical and genetic study of Tunisian families with genetic generalized epilepsy: contribution of CACNA1H and MAST4 genes.
Neurogenetics 2018 6 19 (3): 165-178.
Landoulsi Zied, Laatar Fatma, Noé Eric, Mrabet Saloua, Ben Djebara Mouna, Achaz Guillaume, Nava Caroline, Baulac Stéphanie, Kacem Imen, Gargouri-Berrechid Amina, Gouider Riadh, Leguern Er
Multi-gene panel testing in Korean patients with common genetic generalized epilepsy syndromes.
PloS one 2018 13 (6): e0199321.
Lee Cha Gon, Lee Jeehun, Lee Munhya
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