참고문헌
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피인용 문헌
- Familial hyperkalemic periodic paralysis caused by a de novo mutation in the sodium channel gene SCN4A vol.54, pp.11, 2010, https://doi.org/10.3345/kjp.2011.54.11.470
- Normokalemic periodic paralysis is not a distinct disease vol.46, pp.6, 2010, https://doi.org/10.1002/mus.23441
- Cloning and expression of the two new variants of Nav1.5/SCN5A in rat brain vol.365, pp.1, 2010, https://doi.org/10.1007/s11010-012-1253-7
- The large-conductance calcium-activated potassium channel holds the key to the conundrum of familial hypokalemic periodic paralysis vol.57, pp.10, 2014, https://doi.org/10.3345/kjp.2014.57.10.445
- Gating pore currents are defects in common with two Na v 1.5 mutations in patients with mixed arrhythmias and dilated cardiomyopathy vol.145, pp.2, 2010, https://doi.org/10.1085/jgp.201411304
- Mutation analysis of CACNA1S and SCN4A in patients with hypokalemic periodic paralysis vol.12, pp.4, 2010, https://doi.org/10.3892/mmr.2015.4201
- N1366S mutation of human skeletal muscle sodium channel causes paramyotonia congenita : NaV1.4 defect in PMC vol.595, pp.22, 2010, https://doi.org/10.1113/jp274877
- Na V 1.4 DI-S4 periodic paralysis mutation R222W enhances inactivation and promotes leak current to attenuate action potentials and depolarize muscle fibers vol.8, pp.None, 2018, https://doi.org/10.1038/s41598-018-28594-5