High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.
Fransen E; Verstreken M; Verhagen WI; Wuyts FL; Huygen PL; D'Haese P; Robertson NG; Morton CC; McGuirt WT; Smith RJ; Declau F; Van de Heyning PH; Van Camp G; Human Molecular Genetics, 1999, vol. 8, issue 8, p 1425, ISSN 09646906. ISBN 09646906.

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