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Article

A South African family with the mitochondrial A1555G mutation on haplogroup L0d.

Biochemical and biophysical research communications - 1 May 2009

Human H, Lombard D, de Jong G, Bardien S

Abstract excerpt

The most common mutation associated with aminoglycoside-induced deafness is A1555G and it has been found in diverse populations worldwide. In the present study we investigated a large South African family known to harbour A1555G. A total of 97 family members were genotyped using the SNaPshot tech...

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Source

Identifiers

PMID: 19285484
DOI: 10.1016/j.bbrc.2009.03.032

Genes

GJB2
TRMU
UCN

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19285484-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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