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. 1995 May;56(5):1238–1240.

A mitochondrial mutation at nt 9101 in the ATP synthase 6 gene associated with deficient oxidative phosphorylation in a family with Leber hereditary optic neuroretinopathy.

T Lamminen, A Majander, V Juvonen, M Wikström, P Aula, E Nikoskelainen, M L Savontous
PMCID: PMC1801467  PMID: 7726182

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Selected References

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

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