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. 2013 Aug;120(8):1712-1712.e1.
doi: 10.1016/j.ophtha.2013.04.022.

Dominant optic atrophy: novel OPA1 mutations and revised prevalence estimates

Patrick Yu-Wai-Man  1 , Patrick F Chinnery
Affiliations

Dominant optic atrophy: novel OPA1 mutations and revised prevalence estimates

Patrick Yu-Wai-Man et al. Ophthalmology. 2013 Aug.

Erratum in

  • Ophthalmology. 2013 Dec;120(12):2448
  • Erratum.
    [No authors listed] [No authors listed] Ophthalmology. 2013 Dec;120(12):2448. doi: 10.1016/j.ophtha.2013.09.025. Epub 2013 Nov 15. Ophthalmology. 2013. PMID: 30005548 No abstract available.
No abstract available

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Conflict of interest statement

Financial Disclosures:

All the listed authors in this manuscript report no relevant financial disclosures or conflicts of interest.

References

    1. Yu-Wai-Man P, Griffiths PG, Burke A, et al. The prevalence and natural history of dominant optic atrophy due to OPA1 mutations. Ophthalmology. 2010;117:1538–1546. - PMC - PubMed
    1. Yu-Wai-Man P, Griffiths PG, Chinnery PF. Mitochondrial optic neuropathies - Disease mechanisms and therapeutic strategies. Progress in Retinal and Eye Research. 2011;30:81–114. - PMC - PubMed
    1. Lenaers G, Hamel C, Delettre C, et al. Dominant optic atrophy. Orphanet Journal of Rare Diseases. 2012;7:46. - PMC - PubMed
    1. Yu-Wai-Man P, Griffiths PG, Gorman GS, et al. Multi-system neurological disease is common in patients with OPA1 mutations. Brain. 2010;133:771–786. - PMC - PubMed
    1. Thiselton DL, Alexander C, Morris A, et al. A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect. Human Genetics. 2001;109:498–502. - PubMed

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