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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
Alžběta Vondráčková, Kateřina Veselá, Hana Kratochvílová, Vendula Kučerová Vidrová, Kamila Vinšová, Viktor Stránecký, Tomáš Honzík, Hana Hansíková, Jiří Zeman, Markéta Tesařová
Eur J Hum Genet. 2014 Mar; 22(3): 431–434. Published online 2013 Jul 10. doi: 10.1038/ejhg.2013.148
PMCID:
PMC3925276
AbstractArticlePDF–289K

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