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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Nov 8, 2024. (Total: 233355Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Epilepsy and STX1A[original query]
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy.
Annals of neurology 2009 Jun 65 (6): 748-53.
Hamdan Fadi F, Piton Amélie, Gauthier Julie, Lortie Anne, Dubeau François, Dobrzeniecka Sylvia, Spiegelman Dan, Noreau Anne, Pellerin Stéphanie, Côté Mélanie, Henrion Edouard, Fombonne Eric, Mottron Laurent, Marineau Claude, Drapeau Pierre, Lafrenière Ronald G, Lacaille Jean Claude, Rouleau Guy A, Michaud Jacques
Synergistic association of STX1A and VAMP2 with cryptogenic epilepsy in North Indian population.
Brain and behavior 2016 Jul 6 (7): e00490.
Baghel Ruchi, Grover Sandeep, Kaur Harpreet, Jajodia Ajay, Parween Shama, Sinha Juhi, Srivastava Ankit, Srivastava Achal Kumar, Bala Kiran, Chandna Puneet, Kushwaha Suman, Agarwal Rachna, Kukreti Ritushr
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