RNASEH1 mutations impair mtDNA replication, cause adult-onset mitochondrial encephalomyopathy

Saturday, June 27, 2015 - 14:00 in Biology & Nature

Next Generation Sequencing (NGS) technology offers an incredible opportunity for the rapid and relatively low-cost characterization of individual genomes, giving us a chance to make a substantial leap ahead in the molecular dissection of all mitochondrial disorders in humans.

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