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

Thomson, J. and Machado, Rajiv and Pauciulo, M. and Morgan, N. and Yacoub, M. and Corris, P. and McNeil, K. and Loyd, J. and Nichols, W. and Trembath, R. (2001) Familial and sporadic primary pulmonary hypertension is caused by BMPR2 gene mutations resulting in haploinsufficiency of the bone morphogenetic protein type II receptor. Journal of Heart and Lung Transplantation, 20 (2). p. 149. ISSN 1053-2498

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Item Type:Article
Item Status:Live Archive

Abstract

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Keywords:Pulmonary hypertension, Gene mutation, Haploinsufficiency, Protein type II receptor
Subjects:C Biological Sciences > C400 Genetics
C Biological Sciences > C431 Medical Genetics
Divisions:College of Science > School of Life Sciences
ID Code:13457
Deposited On:05 Mar 2014 14:49

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