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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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Detalhes bibliográficos
Publicado no:Eur J Transl Myol
Main Authors: Missaglia, Sara, Pegoraro, Valentina, Marozzo, Roberta, Tavian, Daniela, Angelini, Corrado
Formato: Artigo
Idioma:Inglês
Publicado em: PAGEPress Publications, Pavia, Italy 2020
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Acesso em linha: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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