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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Hum Genome Var
Päätekijät: Hara, Hironori, Takeda, Norifumi, Morita, Hiroyuki, Hatano, Masaru, Amiya, Eisuke, Maki, Hisataka, Minatsuki, Shun, Taki, Mizuri, Shiraishi, Yasuyuki, Fujiwara, Takayuki, Maemura, Sonoko, Komuro, Issei
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group 2017
Aiheet:
Data Report
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5397398/
https://ncbi.nlm.nih.gov/pubmed/28480048
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/hgv.2017.10
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