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Article

Sequence variants in host cell factor C1 are associated with Ménière's disease.

Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology - 1 Jun 2008

Vrabec Jeffrey T, Liu Liqian, Li Bingshan, Leal Suzanne M

Abstract excerpt

HYPOTHESIS: There is a genetic basis for the development of Ménière's (MD) disease. BACKGROUND: The cause of MD is unknown, although many potential theories have been proposed. A genetic basis for the disease is suggested by greater prevalence in Caucasians and familial cases that display an auto...

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Source

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Identifiers

PMID: 18520591
DOI: 10.1097/MAO.0b013e318168d23b
PMCID: PMC2757044

Genes

HCFC1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18520591-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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