PubMed (OMIM) for id: 6328

Year	Number of Results
1991	1
1992	1
1994	1
2000	1
2001	1
2013	2
2014	1
2017	1
2018	1
2024	0

1

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. Zaman T, et al. Ann Neurol. 2018 Apr;83(4):703-717. doi: 10.1002/ana.25188. Epub 2018 Mar 30. Ann Neurol. 2018. PMID: 29466837 Free PMC article.

2

SCN3A deficiency associated with increased seizure susceptibility.

Lamar T, Vanoye CG, Calhoun J, Wong JC, Dutton SBB, Jorge BS, Velinov M, Escayg A, Kearney JA. Lamar T, et al. Neurobiol Dis. 2017 Jun;102:38-48. doi: 10.1016/j.nbd.2017.02.006. Epub 2017 Feb 22. Neurobiol Dis. 2017. PMID: 28235671 Free PMC article.

3

Novel SCN3A variants associated with focal epilepsy in children.

Vanoye CG, Gurnett CA, Holland KD, George AL Jr, Kearney JA. Vanoye CG, et al. Neurobiol Dis. 2014 Feb;62:313-22. doi: 10.1016/j.nbd.2013.10.015. Epub 2013 Oct 21. Neurobiol Dis. 2014. PMID: 24157691 Free PMC article.

4

Interstitial 2q24.3 deletion including SCN2A and SCN3A genes in a patient with autistic features, psychomotor delay, microcephaly and no history of seizures.

Celle ME, Cuoco C, Porta S, Gimelli G, Tassano E. Celle ME, et al. Gene. 2013 Dec 15;532(2):294-6. doi: 10.1016/j.gene.2013.09.073. Epub 2013 Sep 28. Gene. 2013. PMID: 24080482

5

Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locus.

Kasai N, Fukushima K, Ueki Y, Prasad S, Nosakowski J, Sugata K, Sugata A, Nishizaki K, Meyer NC, Smith RJ. Kasai N, et al. Gene. 2001 Feb 7;264(1):113-22. doi: 10.1016/s0378-1119(00)00594-1. Gene. 2001. PMID: 11245985

6

Cloning, distribution and functional analysis of the type III sodium channel from human brain.

Chen YH, Dale TJ, Romanos MA, Whitaker WR, Xie XM, Clare JJ. Chen YH, et al. Eur J Neurosci. 2000 Dec;12(12):4281-9. Eur J Neurosci. 2000. PMID: 11122339

7

Targeted gene walking by low stringency polymerase chain reaction: assignment of a putative human brain sodium channel gene (SCN3A) to chromosome 2q24-31.

Malo MS, Srivastava K, Andresen JM, Chen XN, Korenberg JR, Ingram VM. Malo MS, et al. Proc Natl Acad Sci U S A. 1994 Apr 12;91(8):2975-9. doi: 10.1073/pnas.91.8.2975. Proc Natl Acad Sci U S A. 1994. PMID: 8159690 Free PMC article.

8

Three brain sodium channel alpha-subunit genes are clustered on the proximal segment of mouse chromosome 2.

Malo D, Schurr E, Dorfman J, Canfield V, Levenson R, Gros P. Malo D, et al. Genomics. 1991 Jul;10(3):666-72. doi: 10.1016/0888-7543(91)90450-s. Genomics. 1991. PMID: 1679748

9

Primary structure, chromosomal localization, and functional expression of a voltage-gated sodium channel from human brain.

Ahmed CM, Ware DH, Lee SC, Patten CD, Ferrer-Montiel AV, Schinder AF, McPherson JD, Wagner-McPherson CB, Wasmuth JJ, Evans GA, et al. Ahmed CM, et al. Proc Natl Acad Sci U S A. 1992 Sep 1;89(17):8220-4. doi: 10.1073/pnas.89.17.8220. Proc Natl Acad Sci U S A. 1992. PMID: 1325650 Free PMC article.

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