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.