Functional mutations in 5′UTR of the BMPR2 gene identified in Chinese families with pulmonary arterial hypertension

Abstract. Pulmonary arterial hypertension (PAH) is a progressive pulmonary vasculopathy with significant morbidity and mortality. Bone morphogenetic protein receptor type 2 (BMPR2) has been well recognized as the principal gene responsible for heritable and sporadic PAH. Four unrelated Chinese patie...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Pulm Circ
Asıl Yazarlar: Wang, Jian, Zhang, Chenting, Liu, Chunli, Wang, Wei, Zhang, Nuofu, Hadadi, Cyrus, Huang, Junyi, Zhong, Nanshan, Lu, Wenju
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: University of Chicago Press 2016
Konular:
Original Research
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4860546/
https://ncbi.nlm.nih.gov/pubmed/27162618
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1086/685078
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