Channelopathy Genes in Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is a rare, progressive vasculopathy with significant cardiopulmonary morbidity and mortality. The underlying pathogenetic mechanisms are heterogeneous and current therapies aim to decrease pulmonary vascular resistance but no curative treatments are available. C...

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Detalles Bibliográficos
Autores principales: Welch, Carrie L., Chung, Wendy K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961593/
https://www.ncbi.nlm.nih.gov/pubmed/35204766
http://dx.doi.org/10.3390/biom12020265

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961593/
https://www.ncbi.nlm.nih.gov/pubmed/35204766
http://dx.doi.org/10.3390/biom12020265

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