Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency

Sara Missaglia, Daniela Tavian, Laura Moro, Corrado Angelini

Risultato della ricerca: Contributo in rivistaArticolo in rivistapeer review

17 Citazioni (Scopus)

Fingerprint Entra nei temi di ricerca di 'Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency'. Insieme formano una fingerprint unica.

Medicine & Life Sciences

Chemical Compounds