Mutations in NDUFAF3 (C3ORF60), Encoding an NDUFAF4 (C6ORF66)-Interacting Complex I Assembly Protein, Cause Fatal Neonatal Mitochondrial Disease

This publication has 33 references indexed in Scilit:

• STRING 8--a global view on proteins and their functional interactions in 630 organisms
  Nucleic Acids Research, 2008
• Human mitochondrial complex I assembles through the combination of evolutionary conserved modules: a framework to interpret complex I deficiencies
  Human Molecular Genetics, 2004
• Mitochondrial disorders: Prevalence, myths and advances
  Journal of Inherited Metabolic Disease, 2004
• Identification and Characterization of a Common Set of Complex I Assembly Intermediates in Mitochondria from Patients with Complex I Deficiency
  Journal of Biological Chemistry, 2003
• mtDNA depletion myopathy: elucidation of the tissue specificity in the mitochondrial thymidine kinase (TK2) deficiency
  Molecular Genetics and Metabolism, 2003
• Stop and Go Extraction Tips for Matrix-Assisted Laser Desorption/Ionization, Nanoelectrospray, and LC/MS Sample Pretreatment in Proteomics
  Analytical Chemistry, 2002
• SecDFyajC forms a heterotetrameric complex with YidC
  Molecular Microbiology, 2002
• Blue Native electrophoresis to study mitochondrial and other protein complexes
  Methods, 2002
• Dissecting protein–protein recognition sites
  Proteins-Structure Function and Bioinformatics, 2002
• Predicting Protein Function by Genomic Context: Quantitative Evaluation and Qualitative Inferences
  Genome Research, 2000