Article
Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population.
American journal of medical genetics. Part A - 1 Jan 2010
Campbell Colleen A, Della Santina Charley C, Meyer Nicole C, Smith Nancy B, Myrie Oluwaseun A, Stone Edwin M, Fukushima Kuni, Califano Joseph, Carey John P, Hansen Marlan R, Gantz Bruce J, Minor Lloyd B, Smith Richard J H
Abstract excerpt
Ménière disease (MD) is a complex disorder of unknown etiology characterized by the symptom triad of vertigo, sensorineural hearing loss, and tinnitus. Its reported incidence is 1-2 per 1,000 in Caucasians and 0.03-0.37 per 1,000 in Japanese. Doi et al. [Doi et al. (2005); ORL J Otorhinolaryngol...
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