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pubmed-article:12821254pubmed:abstractTextThe 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.lld:pubmed
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pubmed-article:12821254pubmed:articleTitlePrimary pulmonary hypertension may be a heterogeneous disease with a second locus on chromosome 2q31.lld:pubmed
pubmed-article:12821254pubmed:affiliationInstitute of Human Genetics, University of Heidelberg, Germany.lld:pubmed
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