Research on potential biomarkers in hereditary hemorrhagic 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...

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Vydáno v:Front Genet
Hlavní autoři: Botella, Luisa-María, Albiñana, Virginia, Ojeda-Fernandez, Luisa, Recio-Poveda, Lucia, Bernabéu, Carmelo
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2015
Témata:
Pediatrics
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4379940/
https://ncbi.nlm.nih.gov/pubmed/25873934
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2015.00115
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