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Article

Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families.

Clinical genetics - 1 Sept 2013

Lee K, Chiu I, Santos-Cortez R L P, Basit S, Khan S, Azeem Z, Andrade P B, Kim S S, Ahmad W, Leal S M

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Share to Consanguinity
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 23173898
DOI: 10.1111/cge.12047
PMCID: PMC6220893

Genes

OTOA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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