Article
Audiometric, vestibular, and genetic aspects of a DFNA9 family with a G88E COCH mutation.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology - 1 Sept 2005
Kemperman Martijn H, De Leenheer Els M R, Huygen Patrick L M, van Duijnhoven Gerard, Morton Cynthia C, Robertson Nahid G, Cremers Frans P M, Kremer Hannie, Cremers Cor W R J
Abstract excerpt
OBJECTIVES: To perform genetic analysis and to analyze cochleovestibular impairment features in a newly identified Dutch family with nonsyndromic autosomal dominant hearing impairment (DFNA9). STUDY DESIGN: Genetic analysis was performed using microsatellite markers and single nucleotide polymorphisms. Audiometric data were collected and analyzed longitudinally. Results were compared with those obtained in...
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