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Escayg A, Heils A, MacDonald BT, Haug K, Sander T, Meisler MH (2001)
A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy.
68
866
73
2001
Am J Hum Genet
Other categories referring to Escayg A, Heils A, MacDonald BT, Haug K, Sander T, Meisler MH (2001)
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