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• W2040259544 abstract "Abstract Meniere's disease (MD) is characterized by spontaneous attacks of vertigo, fluctuating sensorineural hearing loss, tinnitus, and aural fullness. The majority of patients with MD appear sporadic but 5%–13% of the cases have a family history for the disease. The cause of both the sporadic and inherited forms of MD remains unclear despite a number of candidate genes defined from their association with hearing loss. We have performed a genome wide linkage scan on a large Swedish family segregating MD in five generations. Five candidate regions with a lod score of >1 were identified. Two additional families with autosomal dominant MD were analyzed for linkage to these regions and a cumulative Z max of 3.46 was obtained for a single region on chromosome 12p. In two of the three families, a shared haplotype was found to extend over 1.7 Mb which suggests a common ancestral origin. Within this region, a single recombination event restricts the candidate region to 463 kb. © 2006 Wiley‐Liss, Inc." @default.
• W2040259544 created "2016-06-24" @default.
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• W2040259544 date "2006-06-01" @default.
• W2040259544 modified "2023-10-12" @default.
• W2040259544 title "A Meniere's disease gene linked to chromosome 12p12.3" @default.
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• W2040259544 doi "https://doi.org/10.1002/ajmg.b.30347" @default.
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