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

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Description scientific article
Author/s

author: Antonio Federico  Massimo Zeviani  Edoardo Malfatti  Gian Nicola Gallus  Elena Cardaioli  Alessandro Malandrini  Gianna Berti  Carmen Gaudiano  Federica Invernizzi 

Publication date February 18, 2009
Language English
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