Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Syndrome 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 |
Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort. Heart rhythm : the official journal of the Heart Rhythm Society 2007 Jun 4 (6): 752-5. Koopmann Tamara T, Beekman Leander, Alders Marielle, Meregalli Paola G, Mannens Marcel M A M, Moorman Antoon F M, Wilde Arthur A M, Bezzina Connie |
Mutations in sodium channel ß1- and ß2-subunits associated with atrial fibrillation. Circulation. Arrhythmia and electrophysiology 2009 Jun 2 (3): 268-75. Watanabe Hiroshi, Darbar Dawood, Kaiser Daniel W, Jiramongkolchai Kim, Chopra Sameer, Donahue Brian S, Kannankeril Prince J, Roden Dan |
A novel microsatellite polymorphism of sodium channel beta1-subunit gene (SCN1B) may underlie abnormal cardiac excitation manifested by coved-type ST-elevation compatible with Brugada syndrome in Japanese. International journal of clinical pharmacology and therapeutics 2010 Feb 48 (2): 109-19. Ogawa R, Kishi R, Takagi A, Sakaue I, Takahashi H, Matsumoto N, Masuhara K, Nakazawa K, Kobayashi S, Miyake F, Echizen |
Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy. Epilepsy research 2012 Dec 102 (3): 195-200. Wang Ji-wen, Shi Xiu-yu, Kurahashi Hirokazu, Hwang Su-Kyeong, Ishii Atsushi, Higurashi Norimichi, Kaneko Sunao, Hirose Shinichi, |
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 |
SCN1B and SCN2B gene variants analysis in dravet syndrome patients: Analysis of 22 cases. Medicine 2019 3 98 (13): e14974. Gong Jiao-E, Liao Hong-Mei, Long Hong-Yu, Li Xiang-Min, Long Li-Li, Zhou Luo, Gu Wen-Ping, Lu Shao-Hua, Qu Qiang, Yang Li-Min, Xiao Bo, Qu Ji |
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- Page last updated:Apr 22, 2024
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