دورية أكاديمية

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

التفاصيل البيبلوغرافية
العنوان: A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report
المؤلفون: De Pasquale, LoredanaAff1, IDs1305202201356w_cor1, Meo, Petronilla, Fulia, Francesco, Anania, Antonio, Meli, Valerio, Mondello, Antonina, Raimondo, Maria Tindara, Tulino, Viviana, Coletta, Maria Sole, Cacace, Caterina
المصدر: Italian Journal of Pediatrics. 48(1)
قاعدة البيانات: Springer Nature Journals
الوصف
تدمد:18247288
DOI:10.1186/s13052-022-01356-w