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

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...

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Podrobná bibliografie
Vydáno v:Eur J Transl Myol
Hlavní autoři: Missaglia, Sara, Pegoraro, Valentina, Marozzo, Roberta, Tavian, Daniela, Angelini, Corrado
Médium: Artigo
Jazyk:Inglês
Vydáno: PAGEPress Publications, Pavia, Italy 2020
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7254427/
https://ncbi.nlm.nih.gov/pubmed/32499892
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4081/ejtm.2019.8880
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