Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Meniere's Disease and KCNE1[original query] |
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| A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies. International journal of audiology 2012 Aug . Hietikko E, Kotimäki J, Okuloff A, Sorri M, Männikkö M |
| 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 |
| The Polymorphic Analysis of the Human Potassium Channel KCNE Gene Family in Meniere's Disease-A Preliminary Study. The journal of international advanced otology 2019 Apr 15 (1): 130-134. Dai Qingqing, Wang Dan, Zheng Ho |
- Page last reviewed:Feb 1, 2024
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