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Year | Number of Results |
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2002 | 1 |
2006 | 1 |
2024 | 0 |
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Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy.
Pediatr Neurol. 2006 Feb;34(2):116-20. doi: 10.1016/j.pediatrneurol.2005.07.009.
Pediatr Neurol. 2006.
PMID: 16458823
Molecular and pathological effects of a modifier gene on deficiency of the sodium channel Scn8a (Na(v)1.6).
Kearney JA, Buchner DA, De Haan G, Adamska M, Levin SI, Furay AR, Albin RL, Jones JM, Montal M, Stevens MJ, Sprunger LK, Meisler MH.
Kearney JA, et al.
Hum Mol Genet. 2002 Oct 15;11(22):2765-75. doi: 10.1093/hmg/11.22.2765.
Hum Mol Genet. 2002.
PMID: 12374766
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