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Screening Consanguineous Families for Hearing Loss Using the MiamiOtoGenes Panel.

Genetic testing and molecular biomarkers - 1 Oct 2020

Kannan-Sundhari Abhiraami, Yan Denise, Saeidi Kolsoum, Sahebalzamani Afsaneh, Blanton Susan H, Liu Xue Zhong

Abstract excerpt

Background: Hearing loss (HL) is one of the most common and genetically heterogeneous sensory disorders in humans. Genetic causes underlie 50-60% of all HL and the majority of these cases exhibit an autosomal recessive model of inheritance. Methods: In our study, we used our targeted custom MiamiOtoGenes panel of 180 HL-associated genes to screen 23 unrelated consanguineous Iranian families with at least two...

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Identifiers

PMID: 32991204
DOI: 10.1089/gtmb.2020.0153
PMCID: PMC7585618

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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