Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Vertigo and KCNE1[original query] |
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Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population. American journal of medical genetics. Part A 2010 Jan 152A (1): 1. Campbell CA, Della Santina CC, Meyer NC, Smith NB, Myrie OA, Stone EM, Fukushima K, Califano J, Carey JP, Hansen MR, Gantz BJ, Minor LB, Smith RJ |
Ménière's Disease: Molecular Analysis of Aquaporins 2, 3 and Potassium Channel KCNE1 Genes in Brazilian Patients. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2016 09 37 (8): 1117-21. Lopes Karen de Carvalho, Sartorato Edi Lúcia, da Silva-Costa Sueli M, de Macedo Adamov Nadya Soares, Ganança Fernando Freit |
Variants in the KCNE1 or KCNE3 gene and risk of Ménière's disease: A meta-analysis. Journal of vestibular research : equilibrium & orientation 2016 Jan 25 (5-6): 211-8. Li Yuan-Jun, Jin Zhan-Guo, Xu Xian-Ro |
Genetic Susceptibility Study of Chinese Sudden Sensorineural Hearing Loss Patients with Vertigo. Current medical science 2021 Aug 41 (4): 673-679. Gao Yun, Wang Hong-Yang, Guan Jing, Lan Lan, Zhao Cui, Xie Lin-Yi, Wang Da-Yong, Wang Qiu- |
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