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Global metabolic profiling reveals metabolic consequences of mitochondrial coenzyme A deficiency in patients with PANK2 mutations
Authors:Laura Strittmatter  Valerio Leoni  Giovanna Zorzi  Federica Zibordi  Sabrina Dusi  Barbara Garavaglia  Paola Venco  Claudio Caccia  Amanda L. Souza  Amy Deik  Clary B. Clish  Marco Rimoldi  Emilio Ciusani  Enrico Bertini  Nardo Nardocci  Vamsi K. Mootha  Valeria Tiranti
Affiliation:1. Departments of Systems Biology and Medicine, Harvard Medical School and Massachusetts General Hospital, Boston, MA 02114, USA;2. Broad Institute, Cambridge, MA 02142, USA;3. Laboratory of Clinical Pathology and Medical Genetics IRCCS Foundation Neurological Institute “C.Besta”, Milan, Italy;4. Unit of Child Neurology IRCCS Foundation Neurological Institute “C.Besta”, Milan, Italy;5. Unit of Molecular Neurogenetics, Pierfranco and Luisa Mariani Center for the study of Mitochondrial Disorders in Children, IRCCS Foundation Neurological Institute “C.Besta”, Milan, Italy;6. Unit of Molecular Medicine, Department of Neurosciences, Bambino Gesù Pediatric Research Hospital, Rome, Italy
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