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Article

Nonsyndromic hearing loss caused by a mitochondrial T7511C mutation.

The Laryngoscope - 1 Aug 2002

Ishikawa Kotaro, Tamagawa Yuya, Takahashi Katsumasa, Kimura Hiroshi, Kusakari Jun, Hara Akira, Ichimura Keiichi

Abstract excerpt

OBJECTIVES: The aims of the present study were to identify a mutation in a Japanese family showing nonsyndromic sensorineural hearing loss and to relate the mutation to characteristics of patients, including audiovestibular findings. STUDY DESIGN: Familial cohort study. METHODS: Mutation analysis was performed using genomic DNA extracted from blood samples. Subjects underwent audiovestibular examinations,...

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Source

Identifiers

PMID: 12172268
DOI: 10.1097/00005537-200208000-00030

Genes

UCN

Provenance

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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