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A novel heteroplasmic mutation in the mitochondrial ATP6 gene associated with Parkinson's syndrome and epilepsy

✍ Scribed by Baumgartner, A.; Nia, S.; Erdler, M.; Lackmayer, K.; Baumgartner, C.; Schmidt, W.M.; Bittner, R.E.

No coin nor oath required. For personal study only.

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