ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteins

. 2018 Oct 15;27(20):3650.

doi: 10.1093/hmg/ddy273.

Affiliations

¹ Laboratory of Molecular Medicine, Unit of Muscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
² Institut für Zytobiologie, Philipps-Universität Marburg, Marburg, Germany.
³ Institute of Biomembrane, Bioenergetics and Molecular Biotechnology (IBIOM), National Research Council (CNR), Bari, Italy.
⁴ Laboratory of Biochemistry and Molecular Biology, Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari, Bari, Italy.
⁵ Division of Metabolism, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
⁶ LOEWE Zentrum für Synthetische Mikrobiologie SynMikro, Marburg, Germany.

Alessandra Torraco et al. Hum Mol Genet. 2018.

. 2018 Oct 15;27(20):3650.

doi: 10.1093/hmg/ddy273.

¹ Laboratory of Molecular Medicine, Unit of Muscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
² Institut für Zytobiologie, Philipps-Universität Marburg, Marburg, Germany.
³ Institute of Biomembrane, Bioenergetics and Molecular Biotechnology (IBIOM), National Research Council (CNR), Bari, Italy.
⁴ Laboratory of Biochemistry and Molecular Biology, Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari, Bari, Italy.
⁵ Division of Metabolism, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
⁶ LOEWE Zentrum für Synthetische Mikrobiologie SynMikro, Marburg, Germany.

No abstract available

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