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PDF Availablehttps://doi.org/10.1136/thx.2010.150953.4
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Cite Journal: Thorax |  Publication Date: Nov 16, 2010 |
BackgroundMutations in bone morphogenetic protein receptor II (BMPR-II) have been shown to underlie most heritable cases of Pulmonary arterial hypertension (PAH). However, less than half the individuals who harbour mutations...
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