Circulating microRNA Associated to Different Stages of Liver Steatosis in Prader–Willi Syndrome and Non-Syndromic Obesity

Background: Prader–Willi syndrome (PWS) is a rare and poorly characterized disease. Recent genomic and transcriptomic studies contributed to elucidate the molecular bases of the syndrome. In this study, we characterized the expression of circulating miRNAs in patients with PWS compared to those with...

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Detalles Bibliográficos
Autores principales: Pratama, Muhammad Yogi, Pascut, Devis, Tamini, Sofia, Minocci, Alessandro, Tiribelli, Claudio, Grugni, Graziano, Sartorio, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7230920/
https://www.ncbi.nlm.nih.gov/pubmed/32295264
http://dx.doi.org/10.3390/jcm9041123

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7230920/
https://www.ncbi.nlm.nih.gov/pubmed/32295264
http://dx.doi.org/10.3390/jcm9041123

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