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Article

Association of the FBXO11 gene with chronic otitis media with effusion and recurrent otitis media: the Minnesota COME/ROM Family Study.

Archives of otolaryngology--head & neck surgery - 1 Jul 2006

Segade Fernando, Daly Kathleen A, Allred Dax, Hicks Pamela J, Cox Miranda, Brown Mark, Hardisty-Hughes Rachel E, Brown Steve D M, Rich Stephen S, Bowden Donald W

Abstract excerpt

OBJECTIVE: The FBXO11 gene is the human homologue of the gene mutated in the novel deaf mouse mutant jeff (Jf), a single gene model of otitis media. We have evaluated single nucleotide polymorphisms (SNPs) in the FBXO11 gene for association with chronic otitis media with effusion/recurrent otitis media (COME/ROM). DESIGN: A total of 13 SNPs were genotyped across the 98.7 kilobases of genomic DNA encompassing...

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Identifiers

PMID: 16847180
DOI: 10.1001/archotol.132.7.729
PMCID: PMC1904347

Genes

FBXO11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Association of the FBXO11 gene with chronic otitis media with effusion and recurrent otitis media: the Minnesota COME/ROM Family Study.PMID 16847180Read ↗

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