These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
38. Mutations in SCN3A cause early infantile epileptic encephalopathy. Zaman T; Helbig I; Božović IB; DeBrosse SD; Bergqvist AC; Wallis K; Medne L; Maver A; Peterlin B; Helbig KL; Zhang X; Goldberg EM Ann Neurol; 2018 Apr; 83(4):703-717. PubMed ID: 29466837 [TBL] [Abstract][Full Text] [Related]
39. De novo mutations of voltage-gated sodium channel alphaII gene SCN2A in intractable epilepsies. Ogiwara I; Ito K; Sawaishi Y; Osaka H; Mazaki E; Inoue I; Montal M; Hashikawa T; Shike T; Fujiwara T; Inoue Y; Kaneda M; Yamakawa K Neurology; 2009 Sep; 73(13):1046-53. PubMed ID: 19786696 [TBL] [Abstract][Full Text] [Related]
40. Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation. Venkateswaran S; Myers KA; Smith AC; Beaulieu CL; Schwartzentruber JA; ; Majewski J; Bulman D; Boycott KM; Dyment DA Epilepsia; 2014 Jul; 55(7):e75-9. PubMed ID: 24903190 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]