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Article

Candidate locus for a nuclear modifier gene for maternally inherited deafness.

American journal of human genetics - 1 Jun 2000

Bykhovskaya Y, Estivill X, Taylor K, Hang T, Hamon M, Casano R A, Yang H, Rotter J I, Shohat M, Fischel-Ghodsian N

Abstract excerpt

Maternally inherited deafness associated with the A1555G mutation in the mitochondrial 12S ribosomal RNA (rRNA) gene appears to require additional environmental or genetic changes for phenotypic expression. Aminoglycosides have been identified as one such environmental factor. In one large Arab-Israeli pedigree with congenital hearing loss in some of the family members with the A1555G mutation and with no...

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Identifiers

PMID: 10788333
DOI: 10.1086/302914
PMCID: PMC1378050

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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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