Abstract
The pathogenesis of primary pulmonary hypertension (PPH) remains poorly understood. Molecular genetic studies have identified that mutations within the gene BMPR2 on the long arm of chromosome 2 underlie familial PPH. This review explores the significance of the PPH gene identification and examines additional genetic determinants, emphasizing the immediate implications for assessment and management of patients and their relatives
Original language | English |
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Pages (from-to) | 883 - 888 |
Number of pages | 6 |
Journal | Pediatric Research |
Volume | 53 |
Issue number | 6 |
DOIs | |
Publication status | Published - 1 Jun 2003 |