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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
Sodium channels SCN1A, SCN2A and SCN3A in familial autism.
Weiss LA, Escayg A, Kearney JA, Trudeau M, MacDonald BT, Mori M, Reichert J, Buxbaum JD, Meisler MH.
Weiss LA, et al.
Mol Psychiatry. 2003 Feb;8(2):186-94. doi: 10.1038/sj.mp.4001241.
Mol Psychiatry. 2003.
PMID: 12610651
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Gene symbol: SCN8A. Disease: Ataxia. Accession #Hd0520.
Meisler MH, Trudeau MM, Dalton JC, Day JW, Ranum LP.
Meisler MH, et al. Among authors: trudeau mm.
Hum Genet. 2006 Feb;118(6):776.
Hum Genet. 2006.
PMID: 17297687
No abstract available.
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SCNM1, a putative RNA splicing factor that modifies disease severity in mice.
Buchner DA, Trudeau M, Meisler MH.
Buchner DA, et al.
Science. 2003 Aug 15;301(5635):967-9. doi: 10.1126/science.1086187.
Science. 2003.
PMID: 12920299
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High-resolution mapping of the sodium channel modifier Scnm1 on mouse chromosome 3 and identification of a 1.3-kb recombination hot spot.
Buchner DA, Trudeau M, George AL Jr, Sprunger LK, Meisler MH.
Buchner DA, et al.
Genomics. 2003 Oct;82(4):452-9. doi: 10.1016/s0888-7543(03)00152-6.
Genomics. 2003.
PMID: 13679025
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Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation.
Trudeau MM, Dalton JC, Day JW, Ranum LP, Meisler MH.
Trudeau MM, et al.
J Med Genet. 2006 Jun;43(6):527-30. doi: 10.1136/jmg.2005.035667. Epub 2005 Oct 19.
J Med Genet. 2006.
PMID: 16236810
Free PMC article.
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