Differential Expression of Circulating Plasma miRNA-370 and miRNA-10a from Patients with Hereditary Hemorrhagic Telangiectasia

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant, vascular disorder that presents with telangiectases and arteriovenous malformations. HHT is a genetically heterogeneous disorder, involving mutations in endoglin (ENG; HHT1) and activin receptor-like kinase 1 (ACVRL1/ALK1; HHT2) g...

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Detalles Bibliográficos
Autores principales: Ruiz-Llorente, Lidia, Albiñana, Virginia, Botella, Luisa M., Bernabeu, Carmelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565099/
https://www.ncbi.nlm.nih.gov/pubmed/32899377
http://dx.doi.org/10.3390/jcm9092855

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565099/
https://www.ncbi.nlm.nih.gov/pubmed/32899377
http://dx.doi.org/10.3390/jcm9092855

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