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Article

Deafness due to A1555G mitochondrial mutation without use of aminoglycoside.

The Laryngoscope - 1 Jun 2004

Matsunaga Tatsuo, Kumanomido Hiroshi, Shiroma Masae, Ohtsuka Akihiro, Asamura Kenji, Usami Shin-Ichi

Abstract excerpt

OBJECTIVES/HYPOTHESIS: The objective was to clarify the characteristics of deafness associated with the A1555G mutation within mitochondrial 12S ribosomal RNA gene in the absence of aminoglycoside exposure. STUDY DESIGN: Clinical and genetic studies in family members with the A1555G mitochondrial mutation were performed. METHODS: The subjects were 123 maternally related members of a large Japanese family with the...

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PMID: 15179218
DOI: 10.1097/00005537-200406000-00024

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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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