Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Hypokalemia and KCNJ2[original query] |
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A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis.
Journal of human genetics 2012 May 57 (5): 301-4. Jongjaroenprasert Wallaya, Phusantisampan Theerawut, Mahasirimongkol Surakameth, Mushiroda Taisei, Hirankarn Nattiya, Snabboon Thiti, Chanprasertyotin Suwannee, Tantiwong Puntip, Soonthornpun Supamai, Rattanapichart Paninee, Mamanasiri Sunee, Himathongkam Thep, Ongphiphadhanakul Boonsong, Takahashi Atsushi, Kamatani Naoyuki, Kubo Michiaki, Nakamura Yusu |
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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