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Article

Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation.

The Laryngoscope - 1 Apr 1997

Usami S, Abe S, Kasai M, Shinkawa H, Moeller B, Kenyon J B, Kimberling W J

Abstract excerpt

Five Japanese families showing aminoglycoside-induced hearing loss were genetically as well as clinically investigated. A mitochondrial mutation at nucleotide 1555 was found in 28 out of 32 subjects. One hundred American control subjects did not show any evidence of the mutation at nucleotide 1555, suggesting that the 1555 A-->G (A1555G) mitochondrial mutation may be found more frequently among populations in the...

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Identifiers

PMID: 9111378
DOI: 10.1097/00005537-199704000-00011

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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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