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...

Full description

Saved in:
Bibliographic Details
Published in:Hum Genome Var
Main Authors: Hara, Hironori, Takeda, Norifumi, Morita, Hiroyuki, Hatano, Masaru, Amiya, Eisuke, Maki, Hisataka, Minatsuki, Shun, Taki, Mizuri, Shiraishi, Yasuyuki, Fujiwara, Takayuki, Maemura, Sonoko, Komuro, Issei
Format: Artigo
Language:Inglês
Published: Nature Publishing Group 2017
Subjects:
Data Report
Online Access: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
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items