Adult-onset ataxia and polyneuropathy caused by mitochondrial 8993T→C mutation von Rantamäki, Maria T., Soini, Heidi K., Finnilä, Saara M., Majamaa, Kari, Udd, Bjarne

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Phylogenetic Network for European mtDNA von Finnilä, Saara, Lehtonen, Mervi S., Majamaa, Kari

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Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1 von Mee, Lisa, Honkala, Heli, Kopra, Outi, Vesa, Jouni, Finnilä, Saara, Visapää, Ilona, Sang, Tzu-Kang, Jackson, George R., Salonen, Riitta, Kestilä, Marjo, Peltonen, Leena

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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 von Hinttala, Reetta, Kervinen, Marko, Uusimaa, Johanna, Maliniemi, Pilvi, Finnilä, Saara, Rantala, Heikki, Remes, Anne M, Hassinen, Ilmo E, Majamaa, Kari

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Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia von AUTERE, Jaana, MOILANEN, Jukka S, FINNILÄ, Saara, SOININEN, Hilkka, MANNERMAA, Arto, HARTIKAINEN, Päivi, HALLIKAINEN, Merja, MAJAMAA, Kari

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A Mutation in Mitochondrial DNA-Encoded Cytochrome c Oxidase II Gene in a Child With Alpers-Huttenlocher-Like Disease von Uusimaa, Johanna, Finnila, Saara, Vainionpaa, Leena, Karppa, Mikko, Herva, Riitta, Rantala, Heikki, Hassinen, Ilmo E, Majamaa, Kari

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Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22–q24 von Saarela, Janna, Schoenberg Fejzo, Marlena, Chen, Daniel, Finnilä, Saara, Parkkonen, Maikki, Kuokkanen, Satu, Sobel, Eric, Tienari, Pentti J., Sumelahti, Marja-Liisa, Wikström, Juhani, Elovaara, Irina, Koivisto, Keijo, Pirttilä, Tuula, Reunanen, Mauri, Palotie, Aarno, Peltonen, Leena

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Evidence for mtDNA Admixture between the Finns and the Saami von Meinilä, Maria, Finnilä, Saara, Majamaa, Kari

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Molecular Epidemiology of Childhood Mitochondrial Encephalomyopathies in a Finnish Population: Sequence Analysis of Entire mtDNA of 17 Children Reveals Heteroplasmic Mutations in t... von Uusimaa, Johanna, Finnila, Saara, Remes, Anne M, Rantala, Heikki, Vainionpaa, Leena, Hassinen, Ilmo E, Majamaa, Kari

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Molecular Epidemiology of Childhood Mitochondrial Encephalomyopathies in a Finnish Population: Sequence Analysis of Entire mtDNA of 17 Children Reveals Heteroplasmic Mutations in t... von Uusimaa, Johanna, Finnilä, Saara, Remes, Anne M, Rantala, Heikki

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Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL von ANNUNEN-RASILA, Johanna, FINNILÄ, Saara, MYKKÄNEN, Kati, MOILANEN, Jukka S, VEIJOLA, Johanna, PÖYHÖNEN, Minna, VIITANEN, Matti, KALIMO, Hannu, MAJAMAA, Kari

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Mitochondrial DNA sequence variation and mutation rate in patients with CADASIL von Annunen-Rasila, Johanna, Finnilä, Saara, Mykkänen, Kati, Moilanen, Jukka S., Veijola, Johanna, Pöyhönen, Minna, Viitanen, Matti, Kalimo, Hannu, Majamaa, Kari

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Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln von Finnilä, Saara, Autere, Jaana, Lehtovirta, Maarit, Hartikainen, Päivi, Mannermaa, Arto, Soininen, Hilkka, Majamaa, Kari

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Molecular epidemiology of childhood mitochondrial encephalomyopathies in a Finnish population: sequence analysis of entire mtDNA of 17 children reveals heteroplasmic mutations in t... von Uusimaa, Johanna, Finnila, Saara, Remes, Anne M, Rantala, Heikki, Vainionpaa, Leena, Hassinen, Ilmo E, Majamaa, Kari

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