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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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Pubblicato in:Cells
Autori principali: Fazal, Shahood, Bisserier, Malik, Hadri, Lahouaria
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI 2021
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7999465/
https://ncbi.nlm.nih.gov/pubmed/33805595
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells10030638
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