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Ferran Vila-Julià Selected Research

Combined Oxidative Phosphorylation Deficiency 1

1/2022Dysfunctional mitochondrial translation and combined oxidative phosphorylation deficiency in a mouse model of hepatoencephalopathy due to Gfm1 mutations.

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Ferran Vila-Julià Research Topics

Disease

2Mitochondrial Diseases (Mitochondrial Disease)
01/2022 - 06/2021
1Combined Oxidative Phosphorylation Deficiency 1
01/2022
1Rare Diseases (Rare Disease)
10/2021
1Muscular Diseases (Myopathy)
08/2021
1Myopathy with lactic acidosis and sideroblastic anemia
08/2021
1Sideroblastic Anemia
08/2021
1Lactic Acidosis
08/2021

Drug/Important Bio-Agent (IBA)

2EnzymesIBA
01/2022 - 10/2021
1polyacrylamideIBA
01/2022
1Peptide Elongation Factors (Elongation Factor)IBA
01/2022
1Thymidine PhosphorylaseIBA
10/2021
1Tyrosine-tRNA LigaseIBA
08/2021
1Mitochondrial DNA (mtDNA)IBA
06/2021