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Saara Finnilä

University of Oulu

27

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1194

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Variations of mitochondrial DNA polymerase γ in patients with Parkinson’s disease

2013 Journal of Neurology
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Mitochondrial DNA sequence variation in Finnish patients with matrilineal diabetes mellitus

2012 BMC Research Notes
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Analysis of functional consequences of haplogroup J polymorphisms m.4216T > C and m.3866T > C in human MT-ND1: Mutagenesis of homologous positions in Escherichia coli

2010 Mitochondrion
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Cytoskeletal structure in cells harboring two mutations: R133C in NOTCH3 and 5650G>A in mitochondrial DNA.

2007 Mitochondrion
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Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL

2006 Neurogenetics
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Sequence variation in the tRNA genes of human mitochondrial DNA.

2005 Journal of Molecular Evolution
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Adult‐onset ataxia and polyneuropathy caused by mitochondrial 8993T→C mutation

2005 Annals of Neurology
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Hereditary dementia with intracerebral hemorrhages and cerebral amyloid angiopathy

2004 Neurology
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Mitochondrial DNA polymorphisms as risk factors for Parkinson’s disease and Parkinson’s disease dementia

2004 Human Genetics
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Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln

2001 Journal of Medical Genetics
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Citations (27)