Severe encephalopathy associated to pyruvate dehydrogenase mutations and unbalanced coenzyme Q10 content
Claudio Asencio(European Molecular Biology Laboratory), Plácido Navas(Centro Andaluz de Biología del Desarrollo)
Cited by 17
Related Papers
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
|Journal of Clinical Investigation|2011|402
Coenzyme Q10 Supplementation in Aging and Disease
|Frontiers in Physiology|2018|349
A Mutation in Para-Hydroxybenzoate-Polyprenyl Transferase (COQ2) Causes Primary Coenzyme Q10 Deficiency
|The American Journal of Human Genetics|2006|346
Effect of vanillic acid on COQ6 mutants identified in patients with coenzyme Q10 deficiency
|Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease|2013|75
Silica-based solid-phase extraction of cross-linked nucleic acid–bound proteins
|Life Science Alliance|2018|73