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Prevalence of biallelic eukaryotic translation initiation factor 2 α kinase 4 (EIF2AK4) mutations in patients with familial pulmonary capillary haemangiomatosis (PCH)/pulmonary veno-occlusive disease (PVOD) and sporadic PCH/PVOD in the French Pulmonary Hypertension Network Registry. #: from 14 different families.
