Research on Potential Biomarkers in Hereditary Haemorrhagic Telangiectasia

Hereditary Hemorrhagic Telangiectasia (HHT) is a genetically heterogeneous disorder, involving mutations in two predominant genes known as Endoglin (ENG; HHT1) and Activin receptor like kinase 1 (ACVRL1/ALK1; HHT2), as well as in some less frequent genes, such as MADH4/SMAD4 (JP-HHT) or BMP9/GDF2 (H...

Description complète

Enregistré dans:
Détails bibliographiques
Auteurs principaux: Luisa Maria Botella, Virginia eAlbiñana, Luisa eOjeda-Fernandez, Lucia eRecio-Poveda, Carmelo eBernabeu
Format: Artigo
Langue:Inglês
Publié: Frontiers Media S.A. 2015-03-01
Collection:Frontiers in Genetics
Sujets:
miRNA
VEGF
biomarkers
DNA SEQUENCING
endoglin
TGF-β
Accès en ligne:http://journal.frontiersin.org/Journal/10.3389/fgene.2015.00115/full
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires