Human Genome Epidemiology Literature Finder
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Query Trace: Aneurysm and SCN5A[original query] |
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H558R, a common SCN5A polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of SCN5A promoters. Journal of biomedical science 2017 Dec 24 (1): 91. Matsumura Hiroya, Nakano Yukiko, Ochi Hidenori, Onohara Yuko, Sairaku Akinori, Tokuyama Takehito, Tomomori Shunsuke, Motoda Chikaaki, Amioka Michitaka, Hironobe Naoya, Toshishige Masaaki, Takahashi Shinya, Imai Katsuhiko, Sueda Taijiro, Chayama Kazuaki, Kihara Yasu |
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