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A novel BMPR2 mutation with widely disparate heritable pulmonary arterial hypertension clinical phenotype
Mutations in the gene encoding bone morphogenetic protein receptor type II (BMPR2) have been associated with heritable pulmonary arterial hypertension (HPAH), whereas mutations in the gene encoding eukaryotic translation initiation factor 2 alpha kinase 4 (EIF2AK4) are associated with heritable pulm...
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| Publicat a: | Pulm Circ |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
SAGE Publications
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7273341/ https://ncbi.nlm.nih.gov/pubmed/32547734 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2045894020931315 |
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