Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus von Soini, Heidi K, Moilanen, Jukka S, Vilmi-Kerälä, Tiina, Finnilä, Saara, 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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Lineage-specific selection in human mtDNA: lack of polymorphisms in a segment of MTND5 gene in haplogroup J von Moilanen, Jukka S, Finnila, Saara, Majamaa, Kari

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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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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 haplogroup U as a risk factor for occipital stroke in migraine von Majamaa, Kari, Finnila, Saara, Turkka, Jukka, Hassinen, Ilmo E

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POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype von Komulainen, Tuomas, Hinttala, Reetta, Kärppä, Mikko, Pajunen, Leila, Finnilä, Saara, Tuominen, Hannu, Rantala, Heikki, Hassinen, Ilmo, Majamaa, Kari, Uusimaa, Johanna

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Cytoskeletal structure in cells harboring two mutations: R133C in NOTCH3 and 5650G>A in mitochondrial DNA von Annunen-Rasila, Johanna, Kärppä, Mikko, Finnilä, Saara, Ylä-Outinen, Heli, Veijola, Johanna, Tuominen, Hannu, Peltonen, Juha, Majamaa, Kari

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Phylogenetic Network for European mtDNA von Finnilä, Saara, Lehtonen, Mervi S., 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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Mitochondrial DNA sequence variation in Finnish patients with matrilineal diabetes mellitus von Soini, Heidi K, Moilanen, Jukka S, Finnila, Saara, 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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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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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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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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Phylogenetic Network of the mtDNA Haplogroup U in Northern Finland Based on Sequence Analysis of the Complete Coding Region by Conformation-Sensitive Gel Electrophoresis von Finnilä, Saara, Hassinen, Ilmo E., Ala-Kokko, Leena, Majamaa, Kari

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A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASIL von FINNILÄ, Saara, TUISKU, Seppo, HERVA, Riitta, 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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Sequence variation in the tRNA genes of human mitochondrial DNA von Vilmi, Tiina, Moilanen, Jukka S, Finnilä, Saara, Majamaa, Kari

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