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A variable neurodegenerative phenotype with polymerase γ mutation

https://doi.org/10.1136/jnnp.2008.166066

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    Footnotes

    • Funding Department of Neurology, Charité University Medicine Berlin, Helmholtz Gemeinschaft für Forschungseinrichtung. Telethon-Italy no GGP07019.

    • Competing interests None.

    • Patient consent Obtained from the patient's family.

    • Provenance and Peer review Not commissioned; externally peer reviewed.