Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Abnormalities and SCN2B[original query] |
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Mutations of neuronal voltage-gated Na+ channel alpha 1 subunit gene SCN1A in core severe myoclonic epilepsy in infancy (SMEI) and in borderline SMEI (SMEB). Epilepsia 2004 Feb 45 (2): 140-8. Fukuma Goryu, Oguni Hirokazu, Shirasaka Yukiyoshi, Watanabe Kazuyoshi, Miyajima Tasuku, Yasumoto Sawa, Ohfu Masaharu, Inoue Takahito, Watanachai Aruchalean, Kira Ryutaro, Matsuo Muneaki, Muranaka Hideki, Sofue Fumiko, Zhang Bo, Kaneko Sunao, Mitsudome Akihisa, Hirose Shinic |
Is sudden unexplained nocturnal death syndrome in Southern China a cardiac sodium channel dysfunction disorder? Forensic science international 2014 Mar 236 38-45. Liu Chao, Tester David J, Hou Yiding, Wang Wen, Lv Guoli, Ackerman Michael J, Makielski Jonathan C, Cheng Jiandi |
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- Page last updated:Apr 16, 2024
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