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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Front Genet |
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| Κύριοι συγγραφείς: | , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Frontiers Media S.A.
2015
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| Θέματα: | |
| Διαθέσιμο Online: | 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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