Novel EIF2AK4 mutations in histologically proven pulmonary capillary hemangiomatosis and hereditary pulmonary arterial hypertension
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...
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| Main Authors: | , , , , , , |
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| Format: | Book |
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BMC,
2019-11-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |