Vascular deficiency of Smad4 causes arteriovenous malformations: a mouse model of Hereditary Hemorrhagic Telangiectasia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Clinical Biochemistry,Physiology
Link
http://link.springer.com/article/10.1007/s10456-018-9602-0/fulltext.html
Reference67 articles.
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3. Shovlin CL (2010) Hereditary haemorrhagic telangiectasia: pathophysiology, diagnosis and treatment. Blood Rev 24(6):203–219. https://doi.org/10.1016/j.blre.2010.07.001
4. Botella LM, Albinana V, Ojeda-Fernandez L, Recio-Poveda L, Bernabeu C (2015) Research on potential biomarkers in hereditary hemorrhagic telangiectasia. Front Genet 6:115. https://doi.org/10.3389/fgene.2015.00115
5. Sabba C, Pasculli G, Suppressa P, D’Ovidio F, Lenato GM, Resta F, Assennato G, Guanti G (2006) Life expectancy in patients with hereditary haemorrhagic telangiectasia. QJM Mon J Assoc Phys 99(5):327–334. https://doi.org/10.1093/qjmed/hcl037
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