2016
DOI: 10.1002/brb3.490
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Synergistic association of STX1A and VAMP2 with cryptogenic epilepsy in North Indian population

Abstract: Introduction“Common epilepsies”, merely explored for genetics are the most frequent, nonfamilial, sporadic cases in hospitals. Because of their much debated molecular pathology, there is a need to focus on other neuronal pathways including the existing ion channels.MethodsFor this study, a total of 214 epilepsy cases of North Indian ethnicity comprising 59.81% generalized, 40.19% focal seizures, and based on epilepsy types, 17.29% idiopathic, 37.38% cryptogenic, and 45.33% symptomatic were enrolled. Additional… Show more

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Cited by 9 publications
(1 citation statement)
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“…Notably, STX1A was screened out at both prepartum and postpartum. STX1A as a presynaptic protein is widely expressed in brain, endocrine system, heart, and other organs [53]. STX1A has been associated with myocardial ischemia-reperfusion by regulating KATP and calcium channels signaling pathways [54].…”
Section: Discussionmentioning
confidence: 99%
“…Notably, STX1A was screened out at both prepartum and postpartum. STX1A as a presynaptic protein is widely expressed in brain, endocrine system, heart, and other organs [53]. STX1A has been associated with myocardial ischemia-reperfusion by regulating KATP and calcium channels signaling pathways [54].…”
Section: Discussionmentioning
confidence: 99%