Sequencing of mutations in the serine/threonine kinase domain of the bone morphogenetic protein receptor type 2 gene causing pulmonary arterial hypertension

OBJECTIVE: Germline mutations in the bone morphogenetic protein receptor type-2 (BMPR2) gene are considered to be a major risk factor for pulmonary arterial hypertension (PAH). BMPR2 mutations have been reported in 10%–20% of idiopathic PAH and in 80% of familial PAH cases. The aim of this study was...

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Bibliographische Detailangaben
Veröffentlicht in:Anatol J Cardiol
Hauptverfasser: Mutlu, Zeynep, Kayıkçıoğlu, Meral, Nalbantgil, Sanem, Vuran, Özcan, Kemal, Hatice, Moğulkoç, Nesrin, Ertürk, Biray, Onay, Hüseyin, Eroğlu, Zuhal, Kültürsay, Hakan
Format: Artigo
Sprache:Inglês
Veröffentlicht: Kare Publishing 2016
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Original Investigation
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5331396/
https://ncbi.nlm.nih.gov/pubmed/26645265
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/AnatolJCardiol.2015.6297
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