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Neurology|January 23, 2015
Fe/S protein assembly gene IBA57 mutation causes hereditary spastic paraplegiaAlexander Lossos, Claudia Stümpfig, Giovanni Stevanin, et al.Human Molecular Genetics|May 17, 2018
ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteinsAlessandra Torraco, Oliver Stehling, Claudia Stümpfig, et al.Plant Physiology|August 23, 2020
Redox Modification of the Iron-Sulfur Glutaredoxin GRXS17 Activates Holdase Activity and Protects Plants from Heat StressLaura Martins, Johannes Knuesting, Laetitia Bariat, et al.Human Molecular Genetics|March 7, 2013
Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathyNikhita Ajit Bolar, Arnaud Vincent Vanlander, Claudia Wilbrecht, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 15, 2025
Patient-Derived Neurons Exhibit α-Synuclein Pathology and Previously Unrecognized Major Histocompatibility Complex Class I Elevation in Mitochondrial Membrane Protein-Associated NeurodegenerationLeonie M Heger, Leonie Kertess, Clara Kaufhold, et al.Cell Death & Disease|December 10, 2025
A novel mutation in FDX2 provides insights into the pathogenesis of MEOAL mitochondrial neuromuscular diseaseDavide Doni, Deborah Grifagni, Federica Cavion, et al.American Journal of Human Genetics|November 15, 2011
A fatal mitochondrial disease is associated with defective NFU1 function in the maturation of a subset of mitochondrial Fe-S proteinsAleix Navarro-Sastre, Frederic Tort, Oliver Stehling, et al.Nature Metabolism|August 13, 2025
D-cysteine impairs tumour growth by inhibiting cysteine desulfurase NFS1Joséphine Zangari, Oliver Stehling, Sven A Freibert, et al.Brain : a Journal of Neurology|July 17, 2018
A novel complex neurological phenotype due to a homozygous mutation in FDX2Juliana Gurgel-Giannetti, David S Lynch, Anderson Rodrigues Brandão de Paiva, et al.FEBS Letters|September 26, 2020
Structural and functional diversity calls for a new classification of ABC transportersChristoph Thomas, Stephen G Aller, Konstantinos Beis, et al.Pageof 14