Pulmonary Veno-Occlusive Disease and Pulmonary Fibrosis in a Family with EIF2AK4 Pathogenic Variants
Author:
Affiliation:
1. Université Paris–Saclay, AP-HP, INSERM UMR_S 999Le Kremlin Bicêtre, France
2. Sorbonne Université, AP-HPParis, France
3. Université Paris Cité, AP-HP, INSERM UMR-S 1152 PHEREParis, France
Publisher
American Thoracic Society
Link
https://www.atsjournals.org/doi/pdf/10.1165/rcmb.2023-0166LE
Reference9 articles.
1. 2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension
2. EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension
3. Disruption of GCN2 Pathway Aggravates Vascular and Parenchymal Remodeling during Pulmonary Fibrosis
4. Clinical phenotypes and outcomes of heritable and sporadic pulmonary veno-occlusive disease: a population-based study
5. Pulmonary veno-occlusive disease
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