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Published in Prague medical report (01.01.2017)
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Large copy number variations in combination with point mutations in the TYMP and SCO2 genes found in two patients with mitochondrial disorders
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Published in European journal of human genetics : EJHG (01.03.2014)
Published in European journal of human genetics : EJHG (01.03.2014)
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Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I
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Published in BMC pediatrics (29.01.2020)
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Published in Cardiology in the young (01.07.2017)
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Heterozygous deletion of TYMP and SCO2 genes in combination with c.261C > T mutation in TYMP as a cause of MNGIE
Tesařová⁎, Markéta, Vinšová, Kamila, Kučerová, Vendula, Hansíková, Hana, Honzík, Tomáš, Krijt, Jakub, Karásková, Eva, Smolka, Vratislav, Zeman, Jiří
Published in Mitochondrion (01.07.2011)
Published in Mitochondrion (01.07.2011)
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