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American Journal of Human Genetics|August 1, 2017
Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal EncephalopathyFlorence Habarou, Yamina Hamel, Tobias B Haack, et al.Circulation Research|December 28, 2023
Blood Monocyte Phenotype Is A Marker of Cardiovascular Risk in Type 2 DiabetesJean-Baptiste Julla, Diane Girard, Marc Diedisheim, et al.Nature Cell Biology|June 12, 2026
ERO1a fosters glioblastoma aggressiveness and metabolic flexibility by regulating mitochondria-associated membrane dynamicsArthur Bassot, Lola Violy, Lucas Gorka, et al.Pageof 10