Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Muscle Weakness and KCNJ2[original query] |
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Coexistence of Andersen-Tawil Syndrome with Polymorphisms in hERG1 Gene (K897T) and SCN5A Gene (H558R) in One Family. Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2015 Jun . Jagodzi?ska Michalina, Szperl Ma?gorzata, Poni?ska Joanna, Kosiec Agnieszka, Gajda Robert, Kukla Piotr, Biernacka El?bieta Katarzy |
The clinical and genetic features in a cohort of mainland Chinese patients with thyrotoxic periodic paralysis. BMC neurology 2015 15 38. Li Xiaobing, Yao Sheng, Xiang Yining, Zhang Xiaolei, Wu Xiangbing, Luo Laimin, Huang Haihua, Zhu Min, Wan Hui, Hong Daoj |
Novel lincRNA Susceptibility Gene and Its Role in Etiopathogenesis of Thyrotoxic Periodic Paralysis. Journal of the Endocrine Society 2017 Jul 1 (7): 809-815. Melo Maria Clara C, de Souza Janaína S, Kizys Marina M L, Vidi Angela C, Dorta Haron S, Kunii Ilda S, Giannocco Gisele, Carvalheira Gianna, Dias-da-Silva Magnus |
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