Human Genome Epidemiology Literature Finder
Records 1 - 1 (of 1 Records) |
Query Trace: Epilepsy, Absence and SCN1A[original query] |
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A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy. American journal of human genetics 2001 Apr 68 (4): 866-73. Escayg A, Heils A, MacDonald B T, Haug K, Sander T, Meisler M |
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- Page last updated:Jun 02, 2023
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