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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Detalles Bibliográficos
Autores principales: Missaglia, Sara, Pegoraro, Valentina, Marozzo, Roberta, Tavian, Daniela, Angelini, Corrado
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254427/
https://www.ncbi.nlm.nih.gov/pubmed/32499892
http://dx.doi.org/10.4081/ejtm.2019.8880

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254427/
https://www.ncbi.nlm.nih.gov/pubmed/32499892
http://dx.doi.org/10.4081/ejtm.2019.8880

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