Familial and sporadic primary pulmonary hypertension is caused by BMPR2 gene mutations resulting in haploinsufficiency of the bone morphogenetic protein tùype II receptor

✍ Scribed by J. Thomson; R. Machado; M. Pauciulo; N. Morgan; M. Yacoub; P. Corris; K. McNeil; J. Loyd; W. Nichols; R. Trembath

• Book ID: 117709443
• Publisher: Elsevier Science
• Year: 2001
• Tongue: English
• Weight: 101 KB
• Volume: 20
• Category: Article
• ISSN: 1557-3117
• DOI: 10.1016/s1053-2498(01)00259-5