Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Muscle Weakness 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 |
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 |
Genetic spectrum and founder effect of non-dystrophic myotonia: a Japanese case series study. Journal of neurology 2022 7 269 (12): 6406-6415. Yuan Jun-Hui, Higuchi Yujiro, Hashiguchi Akihiro, Ando Masahiro, Yoshimura Akiko, Nakamura Tomonori, Sakiyama Yusuke, Takashima Hiros |
Genetic analysis of 37 cases with primary periodic paralysis in Chinese patients. Orphanet journal of rare diseases 2024 4 19 (1): 160. Xuechao Zhao, Haofeng Ning, Lina Liu, Chaofeng Zhu, Yinghui Zhang, Guifang Sun, Huanan Ren, Xiangdong Ko |
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- Page last updated:Apr 29, 2024
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