Clinical characteristics and survival of Chinese patients diagnosed with pulmonary arterial hypertension who carry BMPR2 or EIF2KAK4 variants

BACKGROUND: Variants in the gene encoding bone morphogenetic protein receptor type II (BMPR2) are the most common genetic cause of pulmonary arterial hypertension (PAH), whereas biallelic variants in the eukaryotic translation initiation factor 2 alpha kinase 4 gene (EIF2AK4) are described in pulmon...

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Detalles Bibliográficos
Autores principales: Zeng, Qixian, Yang, Hang, Liu, Bingyang, Ma, Yanyun, Liu, Zhihong, Chen, Qianlong, Li, Wenke, Luo, Qin, Zhao, Zhihui, Zhou, Zhou, Xiong, Changming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7257189/
https://www.ncbi.nlm.nih.gov/pubmed/32471403
http://dx.doi.org/10.1186/s12890-020-01179-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7257189/
https://www.ncbi.nlm.nih.gov/pubmed/32471403
http://dx.doi.org/10.1186/s12890-020-01179-7

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