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By Hakonen Anna H.   Goffart Steffi   Marjavaara Sanna   Paetau Anders   Cooper Helen   Mattila Kimmo   Lampinen Milla   Sajantila Antti   Lnnqvist Tuula   Spelbrink Johannes N.   Suomalainen Anu  

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Oxford University Press

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Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma

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Human Molecular Genetics, Vol. 17, Iss. 7, 2008-04 ,pp. : 986-995

Oxford University Press

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Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy

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Human Molecular Genetics, Vol. 21, Iss. 20, 2012-10 ,pp. : 4521-4529

Oxford University Press

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Mitochondrial Complex I Deficiency in Humans

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Bentham Science Publishers

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Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and Twinky

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Human Molecular Genetics, Vol. 14, Iss. 20, 2005-10 ,pp. : 2981-2990

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