Clinical characteristics and survival of Chinese patients diagnosed with pulmonary arterial hypertension who carry BMPR2 or EIF2KAK4 variants
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DOI: 10.1186/s12890-020-01179-7
Abstract: 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… read more here.
Keywords: bmpr2 variants; patients bmpr2; eif2ak4 variants; clinical characteristics ... See more keywords