Search Results - Rakosnikova, Tereza

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    Case report: A rare variant m.4135T>C in the MT-ND1 gene leads to Leber hereditary optic neuropathy and altered respiratory chain supercomplexes

    Case report: A rare variant m.4135T>C in the MT-ND1 gene leads to Leber hereditary optic neuropathy and altered respiratory chain supercomplexes by Rákosníková, Tereza, Kelifová, Silvie, Štufková, Hana, Lokvencová, Kateřina, Lišková, Petra, Kousal, Bohdan, Honzík, Tomáš, Hansíková, Hana, Martínek, Václav, Tesařová, Markéta

    Published in Frontiers in genetics
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    Mitochondrial organization and structure are compromised in fibroblasts from patients with Huntington's disease

    Mitochondrial organization and structure are compromised in fibroblasts from patients with Huntington's disease by Vanisova, Marie, Stufkova, Hana, Kohoutova, Michaela, Rakosnikova, Tereza, Krizova, Jana, Klempir, Jiri, Rysankova, Irena, Roth, Jan, Zeman, Jiri, Hansikova, Hana

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    Case report: A rare variant m.4135T>C in the MT-ND1 gene leads to Leber hereditary optic neuropathy and altered respiratory chain supercomplexes

    Case report: A rare variant m.4135T>C in the MT-ND1 gene leads to Leber hereditary optic neuropathy and altered respiratory chain supercomplexes by Rákosníková, Tereza, Kelifová, Silvie, Štufková, Hana, Lokvencová, Kateřina, Lišková, Petra, Kousal, Bohdan, Honzík, Tomáš, Hansíková, Hana, Martínek, Václav, Tesařová, Markéta

    Published in Frontiers in genetics
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