Molecular and Genetic Profiling for Precision Medicines in Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is a rare and chronic lung disease characterized by progressive occlusion of the small pulmonary arteries, which is associated with structural and functional alteration of the smooth muscle cells and endothelial cells within the pulmonary vasculature. Excessive...

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Detalles Bibliográficos
Autores principales: Fazal, Shahood, Bisserier, Malik, Hadri, Lahouaria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999465/
https://www.ncbi.nlm.nih.gov/pubmed/33805595
http://dx.doi.org/10.3390/cells10030638

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999465/
https://www.ncbi.nlm.nih.gov/pubmed/33805595
http://dx.doi.org/10.3390/cells10030638

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