Tobias B. Haack

1. Mutations in FBXL4, Encoding a Mitochondrial Protein, Cause Early-Onset Mitochondrial Encephalomyopathy
   2013/08/29 by Xiaowu Gai, Daniele Ghezzi, Mark A. Johnson +52 · 30 citations
   Biochemistry, Genetics and Molecular Biology · #Mitochondrial Function and Pathology #Ubiquitin and proteasome pathways #Endoplasmic Reticulum Stress and Disease
2. Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy
   2014/11/26 by Robert Kopajtich, Thomas J. Nicholls, Thomas J. Nicholls +62 · 29 citations
   Biochemistry, Genetics and Molecular Biology · #Mitochondrial Function and Pathology #Metabolism and Genetic Disorders #ATP Synthase and ATPases Research
3. Mutations of the Mitochondrial-tRNA Modifier MTO1 Cause Hypertrophic Cardiomyopathy and Lactic Acidosis
   2012/05/17 by Daniele Ghezzi, Enrico Baruffini, Tobias B. Haack +13 · 28 citations
   Biochemistry, Genetics and Molecular Biology · Medicine · #Mitochondrial Function and Pathology #ATP Synthase and ATPases Research #Cardiomyopathy and Myosin Studies
4. TRMT5 Mutations Cause a Defect in Post-transcriptional Modification of Mitochondrial tRNA Associated with Multiple Respiratory-Chain Deficiencies
   2015/07/17 by Christopher A. Powell, Christopher A. Powell, Robert Kopajtich +31 · 27 citations
   Biochemistry, Genetics and Molecular Biology · Medicine · #RNA modifications and cancer #Congenital Heart Disease Studies #Mitochondrial Function and Pathology