A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report

por De Pasquale, Loredana, Meo, Petronilla, Fulia, Francesco, Anania, Antonio, Meli, Valerio, Mondello, Antonina, Raimondo, Maria Tindara, Tulino, Viviana, Coletta, Maria Sole, Cacace, Caterina
Publicado 2022