Correlation between ETFDH mutations and dysregulation of serum myomiRs in MADD patients

• Main Authors: Sara Missaglia (Author), Valentina Pegoraro (Author), Roberta Marozzo (Author), Daniela Tavian (Author), Corrado Angelini (Author)
• Format: Book
• Published: PAGEPress Publications, 2020-03-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Multiple acyl-CoA dehydrogenase deficiency (MADD) is a rare fatty acids oxidation disorder which is often associated with deficiency of electron transfer flavoprotein dehydrogenase (ETFDH). In this study we reported clinical features and evaluation of expression profile of circulating muscle-specifi...