A novel mutation in the mitochondrial tRNAPro gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency

Paola Da Pozzo, Elena Cardaioli, Edoardo Malfatti, Gian Nicola Gallus, Alessandro Malandrini, Carmen Gaudiano, Gianna Berti, Federica Invernizzi, Massimo Zeviani, Antonio Federico

Research output: Contribution to journal › Article › peer-review

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Medicine & Life Sciences