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Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD).

    Citation

    Pilz D, Quarrell OW, Jones EW
    Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD).

    Publication history

    • First published April 1, 1994.
    Online issue publication 
    April 27, 2016

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