Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2003-6-24
pubmed:abstractText
The aim of our study was to identify genetic causes of primary pulmonary hypertension (PPH), to estimate the proportion of families with mutations in the BMPR2 (bone morphogenetic protein receptor type 2) gene, and to examine whether genetic heterogeneity might play a role.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0735-1097
pubmed:author
pubmed:issnType
Print
pubmed:day
18
pubmed:volume
41
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2237-44
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:12821254-Adolescent, pubmed-meshheading:12821254-Adult, pubmed-meshheading:12821254-Aged, pubmed-meshheading:12821254-Aged, 80 and over, pubmed-meshheading:12821254-Blood Pressure, pubmed-meshheading:12821254-Bone Morphogenetic Protein Receptors, Type II, pubmed-meshheading:12821254-Child, pubmed-meshheading:12821254-Chromosomes, Human, Pair 2, pubmed-meshheading:12821254-Exercise Test, pubmed-meshheading:12821254-Female, pubmed-meshheading:12821254-Genetic Heterogeneity, pubmed-meshheading:12821254-Genetic Predisposition to Disease, pubmed-meshheading:12821254-Humans, pubmed-meshheading:12821254-Hypertension, Pulmonary, pubmed-meshheading:12821254-Locus Control Region, pubmed-meshheading:12821254-Male, pubmed-meshheading:12821254-Middle Aged, pubmed-meshheading:12821254-Mutation, pubmed-meshheading:12821254-Pedigree, pubmed-meshheading:12821254-Protein-Serine-Threonine Kinases, pubmed-meshheading:12821254-Pulmonary Artery
pubmed:year
2003
pubmed:articleTitle
Primary pulmonary hypertension may be a heterogeneous disease with a second locus on chromosome 2q31.
pubmed:affiliation
Institute of Human Genetics, University of Heidelberg, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't