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Case Reports
. 2008 Jan;255(1):127-9.
doi: 10.1007/s00415-008-0571-x. Epub 2008 Jan 22.

A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation

Maria Liguori, Antonella La Russa, Ida Manna, Virginia Andreoli, Manuela Caracciolo, Patrizia Spadafora, Rita Cittadella, Aldo Quattrone
Case Reports

A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation

Maria Liguori et al. J Neurol. 2008 Jan.
No abstract available

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References

    1. Cell. 2006 Jul 14;126(1):177-89 - PubMed
    1. Am J Ophthalmol. 2004 Nov;138(5):749-55 - PubMed
    1. Hum Mol Genet. 2001 Jun 15;10(13):1369-78 - PubMed
    1. Acta Ophthalmol Scand. 2005 Jun;83(3):337-46 - PubMed
    1. Ann Neurol. 2005 Dec;58(6):958-63 - PubMed

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