Novel EIF2AK4 mutations in histologically proven pulmonary capillary hemangiomatosis and hereditary pulmonary arterial hypertension

• Váldodahkkit: Ossama K. Abou Hassan (Dahkki), Wiam Haidar (Dahkki), Mariam Arabi (Dahkki), Hadi Skouri (Dahkki), Fadi Bitar (Dahkki), Georges Nemer (Dahkki), Imad Bou Akl (Dahkki)
• Materiálatiipa: Girji
• Almmustuhtton: BMC, 2019-11-01T00:00:00Z.
• Fáttát: article
• Liŋkkat: Connect to this object online.

Abstract Background Pulmonary hypertension (PH) remains one of the rarest and deadliest diseases. Pulmonary Capillary Hemangiomatosis (PCH) is one of the sub-classes of PH. It was identified using histological and molecular tools and is characterized by the proliferation of capillaries into the alve...