Effect of Transcriptional Regulator ID3 on Pulmonary Arterial Hypertension and Hereditary Hemorrhagic Telangiectasia

Pulmonary arterial hypertension (PAH) can be discovered in patients who have a loss of function mutation of activin A receptor-like type 1 (ACVRL1) gene, a bone morphogenetic protein (BMP) type 1 receptor. Additionally, ACVRL1 mutations can lead to hereditary hemorrhagic telangiectasia (HHT), also k...

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Detalles Bibliográficos
Autor principal: Avecilla, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657613/
https://www.ncbi.nlm.nih.gov/pubmed/31380118
http://dx.doi.org/10.1155/2019/2123906

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6657613/
https://www.ncbi.nlm.nih.gov/pubmed/31380118
http://dx.doi.org/10.1155/2019/2123906

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