Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-β family

BACKGROUND—Primary pulmonary hypertension (PPH), resulting from occlusion of small pulmonary arteries, is a devastating condition. Mutations of the bone morphogenetic protein receptor type II gene (BMPR2), a component of the transforming growth factor beta (TGF-β) family which plays a key role in ce...

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Autors principals: Thomson, J., Machado, R., Pauciulo, M., Morgan, N., Humbert, M., Elliott, G., Ward, K., Yacoub, M., Mikhail, G., Rogers, P., Newman, J., Wheeler, L., Higenbottam, T., Gibbs, J, Egan, J., Crozier, A., Peacock, A., Allcock, R., Corris, P., Loyd, J., Trembath, R., Nichols, W.
Format: Article
Idioma:English
Publicat: BMJ Group 2000
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Original Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1757155/
https://ncbi.nlm.nih.gov/pubmed/11015450
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.37.10.741
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https://ncbi.nlm.nih.gov/pmc/articles/PMC1757155/
https://ncbi.nlm.nih.gov/pubmed/11015450
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.37.10.741

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