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American Journal of Human Genetics logoLink to American Journal of Human Genetics
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. 1994 Aug;55(2):410–412.

Pathological significance of the mtDNA COX III mutation at nucleotide pair 9438 in Leber hereditary optic neuropathy.

M D Brown, A Torroni, K Huoponen, Y S Chen, M T Lott, D C Wallace
PMCID: PMC1918366  PMID: 8037217

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Johns D. R., Neufeld M. J. Cytochrome c oxidase mutations in Leber hereditary optic neuropathy. Biochem Biophys Res Commun. 1993 Oct 29;196(2):810–815. doi: 10.1006/bbrc.1993.2321. [DOI] [PubMed] [Google Scholar]

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