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4. Depletion of mitochondrial DNA in fibroblast cultures from patients with POLG1 mutations is a consequence of catalytic mutations. Ashley N; O'Rourke A; Smith C; Adams S; Gowda V; Zeviani M; Brown GK; Fratter C; Poulton J Hum Mol Genet; 2008 Aug; 17(16):2496-506. PubMed ID: 18487244 [TBL] [Abstract][Full Text] [Related]
5. Acute liver failure after valproate exposure in patients with POLG1 mutations and the prognosis after liver transplantation. Hynynen J; Komulainen T; Tukiainen E; Nordin A; Arola J; Kälviäinen R; Jutila L; Röyttä M; Hinttala R; Majamaa K; Mäkisalo H; Uusimaa J Liver Transpl; 2014 Nov; 20(11):1402-12. PubMed ID: 25065347 [TBL] [Abstract][Full Text] [Related]
6. POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype. Komulainen T; Hinttala R; Kärppä M; Pajunen L; Finnilä S; Tuominen H; Rantala H; Hassinen I; Majamaa K; Uusimaa J BMC Neurol; 2010 May; 10():29. PubMed ID: 20438629 [TBL] [Abstract][Full Text] [Related]
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