Diagnosis, genetic characterization and clinical follow up of mitochondrial fatty acid oxidation disorders in the new era of expanded newborn screening: A single centre experience

Bibliographic Details
Title: Diagnosis, genetic characterization and clinical follow up of mitochondrial fatty acid oxidation disorders in the new era of expanded newborn screening: A single centre experience
Authors: Maguolo, A., Rodella, G., Dianin, A., Nurti, R., Monge, I., Rigotti, E., Cantalupo, G., Salviati, L., Tucci, S., Pellegrini, F., Molinaro, G., Lupi, F., Tonin, P., Pasini, A., Campostrini, N., Ion Popa, F., Teofoli, F., Vincenzi, M., Camilot, M., Piacentini, G., Bordugo, A.
Source: In Molecular Genetics and Metabolism Reports September 2020 24
Database: ScienceDirect
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ISSN:22144269
DOI:10.1016/j.ymgmr.2020.100632
Published in:Molecular Genetics and Metabolism Reports
Language:English