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

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

Authors

    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).
    Journal of Medical Genetics 1994;31:328-330.

    Publication history

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

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