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Article

3p-- syndrome defines a hearing loss locus in 3p25.3.

Hearing research - 1 Feb 2007

McCullough Brendan J, Adams Joe C, Shilling Dustin J, Feeney M Patrick, Sie Kathleen C Y, Tempel Bruce L

Abstract excerpt

Deletions affecting the terminal end of chromosome 3p result in a characteristic set of clinical features termed 3p-- syndrome. Bilateral, sensorineural hearing loss (SNHL) has been found in some but not all cases, suggesting the possibility that it is due to loss of a critical gene in band 3p25. To date, no genetic locus in this region has been shown to cause human hearing loss. However, the ATP2B2 gene is...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 17208398
DOI: 10.1016/j.heares.2006.11.006
PMCID: PMC1995240

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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