Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Tinnitus 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 |
| Analysis of inner ear potassium recycling genes as potential factors associated with tinnitus. International journal of occupational medicine and environmental health 2012 Sep 25 (4): 356-64. Pawe?czyk Ma?gorzata, Rajkowska El?bieta, Koty?o Piotr, Dudarewicz Adam, Van Camp Guy, ?liwi?ska-Kowalska Mario |
| An Examination of KCNE1 Mutations and Common Variants in Chronic Tinnitus. Genes 2014 4 1 (1): 23-37. Sand Philipp G, Luettich Alexander, Kleinjung Tobias, Hajak Goeran, Langguth Bertho |
| 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 |
| Association Analysis of Candidate Gene Polymorphisms and Tinnitus in Young Musicians. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2021 Jul . Bhatt Ishan Sunilkumar, Dias Raquel, Torkamani A |
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