Three novel BMPR2 mutations associated with advanced pulmonary arterial hypertension

Mutations in the bone morphogenetic protein receptor type II (BMPR2) gene may result in the development of pulmonary arterial hypertension (PAH). However, the contribution of disease-causing mutations to the disease characteristics and responsiveness to recent treatment remains to be elucidated. We...

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Detalles Bibliográficos
Autores principales: Hara, Hironori, Takeda, Norifumi, Morita, Hiroyuki, Hatano, Masaru, Amiya, Eisuke, Maki, Hisataka, Minatsuki, Shun, Taki, Mizuri, Shiraishi, Yasuyuki, Fujiwara, Takayuki, Maemura, Sonoko, Komuro, Issei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Data Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397398/
https://www.ncbi.nlm.nih.gov/pubmed/28480048
http://dx.doi.org/10.1038/hgv.2017.10

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397398/
https://www.ncbi.nlm.nih.gov/pubmed/28480048
http://dx.doi.org/10.1038/hgv.2017.10

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