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Article

Multiple origins of a mitochondrial mutation conferring deafness.

Genetics - 1 Mar 1997

Hutchin T P, Cortopassi G A

Abstract excerpt

A point mutation (1555G) in the smaller ribosomal subunit of the mitochondrial DNA (mtDNA) has been associated with maternally inherited traits of hypersensitivity to streptomycin and sensorineural deafness in a number of families from China, Japan, Israel, and Africa. To determine whether this d...

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Identifiers

PMID: 9055086
DOI: 10.1093/genetics/145.3.771
PMCID: PMC1207861

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-9055086-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Multiple origins of a mitochondrial mutation conferring deafness.PMID 9055086Read ↗

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