| 1 | ATFB12, SCN3B
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| Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population.
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| Wang P, Yang Q, Wu X, Yang Y, Shi L, Wang C, Wu G, Xia Y, Yang B, Zhang R, Xu C, Cheng X, Li S, Zhao Y, Fu F, Liao Y, Fang F, Chen Q, Tu X, Wang QK.
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| Biochem Biophys Res Commun 398(1):98-104. Epub 2010 Jun 15.PMID: 20558140 2010
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| 2 | SCN3B
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| Scn3b knockout mice exhibit abnormal sino-atrial and cardiac conduction properties.
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| Hakim P, Brice N, Thresher R, Lawrence J, Zhang Y, Jackson AP, Grace AA, Huang CL.
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| Acta Physiol (Oxf) 198(1):47-59. Epub 2009 Oct 1.PMID: 19796257 2010
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| 3 | SCN3B
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| Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation.
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| Valdivia CR, Medeiros-Domingo A, Ye B, Shen WK, Algiers TJ, Ackerman MJ, Makielski JC.
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| Cardiovasc Res 86(3):392-400. Epub 2009 Dec 30.PMID: 20042427 2010
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| 4 | BRGS7, SCN3B
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| A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype.
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| Hu D, Barajas-Martinez H, Burashnikov E, Springer M, Wu Y, Varro A, Pfeiffer R, Koopmann TT, Cordeiro JM, Guerchicoff A, Pollevick GD, Antzelevitch C.
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| Circ Cardiovasc Genet 2(3):270-8. Epub 2009 Apr 21.PMID: 20031595 2009
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| 5 | BRGS1, BRGS10, BRGS2, BRGS3, BRGS4, BRGS5, BRGS6, BRGS7, BRGS9, CACN2B, CACNA1C, GPD1L, KCNE3, SCN1B, SCN3B, SCN5A
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| The genetic basis of Brugada syndrome: a mutation update.
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| Hedley PL, Jørgensen P, Schlamowitz S, Moolman-Smook J, Kanters JK, Corfield VA, Christiansen M.
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| Hum Mutat 30(9):1256-66. Review.PMID: 19606473 2009
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| 6 | SCN3b
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| Hippocampal Nabeta3 expression in patients with temporal lobe epilepsy.
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| van Gassen KL, de Wit M, van Kempen M, van der Hel WS, van Rijen PC, Jackson AP, Lindhout D, de Graan PN.
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| Epilepsia 50(4):957-62. Epub 2009 Jan 26.PMID: 19385982 2009
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| 7 | SCN3B
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| Scn3b knockout mice exhibit abnormal ventricular electrophysiological properties.
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| Hakim P, Gurung IS, Pedersen TH, Thresher R, Brice N, Lawrence J, Grace AA, Huang CL.
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| Prog Biophys Mol Biol 98(2-3):251-66. Epub 2009 Jan 24.PMID: 19351516 2008
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| 8 | ABHD10, AP1AR, APH1B, C12orf25, C12orf29, C15orf44, C16orf48, C16orf53, C19orf47, C20orf132, C3orf23, C4orf27, C4orf40, C6orf89, CNST, CYB5R4, DEPDC7, DEPTOR, EFCAB7, FAM172A, FAM192A, GASK1B, GPR155, KIAA1826, LMAN2L, LYSMD3, MAP11, MIG3, MPC2, NNT, RAB1A, SCN3B, SERP1, SNN, SPRTN, TMPRSS11B
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| The LIFEdb database in 2006.
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| Mehrle A, Rosenfelder H, Schupp I, del Val C, Arlt D, Hahne F, Bechtel S, Simpson J, Hofmann O, Hide W, Glatting KH, Huber W, Pepperkok R, Poustka A, Wiemann S.
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| Nucleic Acids Res 34(Database issue):D415-8. 2006
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| 9 | SCN3B
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| Identification of SCN3B as a novel p53-inducible proapoptotic gene.
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| Adachi K, Toyota M, Sasaki Y, Yamashita T, Ishida S, Ohe-Toyota M, Maruyama R, Hinoda Y, Saito T, Imai K, Kudo R, Tokino T.
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| Oncogene 23(47):7791-8. 2004
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| 10 | SCN3B
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| beta 3: an additional auxiliary subunit of the voltage-sensitive sodium channel that modulates channel gating with distinct kinetics.
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| Morgan K, Stevens EB, Shah B, Cox PJ, Dixon AK, Lee K, Pinnock RD, Hughes J, Richardson PJ, Mizuguchi K, Jackson AP.
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| Proc Natl Acad Sci U S A 97(5):2308-13. 2000
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