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 (<i>ENG</i>; HHT1) and activin receptor-like kinase 1 (&...

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Bibliographic Details
Main Authors: Lidia Ruiz-Llorente, Virginia Albiñana, Luisa M. Botella, Carmelo Bernabeu
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Journal of Clinical Medicine
Subjects:
Online Access:https://www.mdpi.com/2077-0383/9/9/2855