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| pubmed-article:15687131 | pubmed:dateCreated | 2005-2-2 | lld:pubmed |
| pubmed-article:15687131 | pubmed:abstractText | Pulmonary arterial hypertension (PAH) is a potentially fatal vasculopathy that can develop at any age. Adult-onset disease has previously been associated with mutations in BMPR2 and ALK-1. Presentation in early life may be associated with congenital heart disease but frequently is idiopathic. | lld:pubmed |
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| pubmed-article:15687131 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15687131 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:15687131 | pubmed:issn | 1524-4539 | lld:pubmed |
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| pubmed-article:15687131 | pubmed:issnType | Electronic | lld:pubmed |
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| pubmed-article:15687131 | pubmed:owner | NLM | lld:pubmed |
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| pubmed-article:15687131 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:15687131 | pubmed:articleTitle | Transforming growth factor-beta receptor mutations and pulmonary arterial hypertension in childhood. | lld:pubmed |
| pubmed-article:15687131 | pubmed:affiliation | Division of Medical Genetics, University of Leicester, Leicester, UK. | lld:pubmed |
| pubmed-article:15687131 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15687131 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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