Paola Arzuffi
Qiagen (United Kingdom)(GB)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, ATP Synthase and ATPases Research, Genomics and Phylogenetic Studies, Genetic Neurodegenerative Diseases
Most-Cited Works
- → Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies(2011)172 cited
- → Sym1, the yeast ortholog of the MPV17 human disease protein, is a stress-induced bioenergetic and morphogenetic mitochondrial modulator(2009)75 cited
- → Partial tandem duplication of mtDNA–tRNAPhe impairs mtDNA translation in late-onset mitochondrial myopathy(2012)2 cited
- → A newly discovered protein is responsible for a progressive mitochondrial encephalomyopathy associated with severe complex III deficiency(2011)
- → Using the GeneReader NGS system and QIAact lung all-in-one assay to detect complex mutations and fusions.(2018)