The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family.

Source:http://linkedlifedata.com/resource/pubmed/id/17723226

Biochem. Biophys. Res. Commun. 2007 Oct 26 362 3 670-6

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PMID
17723226