Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and SCN4A[original query] |
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| Absence of ion channels CACN1AS and SCN4A mutations in thyrotoxic hypokalemic periodic paralysis. Thyroid : official journal of the American Thyroid Association 2004 Mar 14 (3): 187-90. Ng WY, Lui KF, Thai AC, Cheah JS |
| SCN4A variants and Brugada syndrome: phenotypic and genotypic overlap between cardiac and skeletal muscle sodium channelopathies. European journal of human genetics : EJHG 2015 Jun . Bissay Véronique, Van Malderen Sophie C H, Keymolen Kathelijn, Lissens Willy, Peeters Uschi, Daneels Dorien, Jansen Anna C, Pappaert Gudrun, Brugada Pedro, De Keyser Jacques, Van Dooren Son |
| Novel susceptibility gene for nonfamilial hypokalemic periodic paralysis. Neurology 2016 Mar . Song I-Wen, Sung Chih-Chien, Chen Chien-Hsiun, Cheng Chih-Jen, Yang Sung-Sen, Chou Yi-Chun, Yang Jenn-Hwai, Chen Yuan-Tsong, Wu Jer-Yuarn, Lin Shih-H |
| Effects of S906T polymorphism on the severity of a novel borderline mutation I692M in Na 1.4 cause periodic paralysis. Clinical genetics 2016 Oct . Fan Chunxiang, Mao Ninghui, Lehmann-Horn Frank, Bürmann Jan, Jurkat-Rott Kar |
| Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study. Lancet (London, England) 2018 4 391 (10129): 1483-1492. Männikkö Roope, Wong Leonie, Tester David J, Thor Michael G, Sud Richa, Kullmann Dimitri M, Sweeney Mary G, Leu Costin, Sisodiya Sanjay M, FitzPatrick David R, Evans Margaret J, Jeffrey Iona J M, Tfelt-Hansen Jacob, Cohen Marta C, Fleming Peter J, Jaye Amie, Simpson Michael A, Ackerman Michael J, Hanna Michael G, Behr Elijah R, Matthews Em |
| Myotonia congenita: mutation spectrum of CLCN1 in Spanish patients. Journal of genetics 2019 9 98 . Milla Carmen Palma, De Castro Carmen Prior, Gómez-González Clara, Martínez-Montero Paloma, Pascual Pascual Samuel I, Molano Mateos Jes |
| Identification of gene mutations in patients with primary periodic paralysis using targeted next-generation sequencing. BMC neurology 2019 5 19 (1): 92. Luo Sushan, Xu Minjie, Sun Jian, Qiao Kai, Song Jie, Cai Shuang, Zhu Wenhua, Zhou Lei, Xi Jianying, Lu Jiahong, Ni Xiaohua, Dou Tonghai, Zhao Chong |
| Association study in Mexican patients with thyrotoxic hypokalemic periodic paralysis. Biomedical reports 2020 Oct 13 (4): 24. Bautista-Medina Mario Arturo, Gallardo-Blanco Hugo Leonid, Martinez-Garza Laura Elia, Cerda-Flores Ricardo Martin, Lavalle-Gonzalez Fernando Javier, Villarreal-Perez Jesus Zacari |
| Analysis of the genetic background associated with sporadic periodic paralysis in Japanese patients. Journal of the neurological sciences 2020 Mar 116795. Nakaza Maki, Kitamura Yuri, Furuta Mitsuru, Kubota Tomoya, Sasaki Ryogen, Takahashi Masanori |
- Page last reviewed:Feb 1, 2024
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