Harvard Catalyst Profiles

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High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.

High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene. Hum Mol Genet. 1999 Aug; 8(8):1425-9.

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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.