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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
2001-7-23
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pubmed:abstractText |
Most patients with primary pulmonary hypertension are thought to have sporadic, not inherited, disease. Because clinical disease develops in only 10 to 20 percent of persons carrying the gene for familial primary pulmonary hypertension, we hypothesized that many patients with apparently sporadic primary pulmonary hypertension may actually have familial primary pulmonary hypertension.
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pubmed:grant |
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0028-4793
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
2
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pubmed:volume |
345
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
319-24
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:11484688-Adult,
pubmed-meshheading:11484688-Bone Morphogenetic Protein Receptors, Type II,
pubmed-meshheading:11484688-Bone Morphogenetic Proteins,
pubmed-meshheading:11484688-Chromosome Mapping,
pubmed-meshheading:11484688-Chromosomes, Human, Pair 2,
pubmed-meshheading:11484688-Diagnostic Errors,
pubmed-meshheading:11484688-Female,
pubmed-meshheading:11484688-Heterozygote,
pubmed-meshheading:11484688-Humans,
pubmed-meshheading:11484688-Hypertension, Pulmonary,
pubmed-meshheading:11484688-Male,
pubmed-meshheading:11484688-Mutation, Missense,
pubmed-meshheading:11484688-Pedigree,
pubmed-meshheading:11484688-Point Mutation,
pubmed-meshheading:11484688-Protein-Serine-Threonine Kinases
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pubmed:year |
2001
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pubmed:articleTitle |
Mutation in the gene for bone morphogenetic protein receptor II as a cause of primary pulmonary hypertension in a large kindred.
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pubmed:affiliation |
Center for Lung Research, Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN, USA. john.newman@med.va.gov
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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