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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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Détails bibliographiques
Publié dans:J Clin Med
Auteurs principaux: Ruiz-Llorente, Lidia, Albiñana, Virginia, Botella, Luisa M., Bernabeu, Carmelo
Format: Artigo
Langue:Inglês
Publié: MDPI 2020
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC7565099/
https://ncbi.nlm.nih.gov/pubmed/32899377
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm9092855
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