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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Detalles Bibliográficos
Autores principales: Oriaku, Ifeoma, LeSieur, Mallory N., Nichols, William C., Barrios, Roberto, Elliott, C. Gregory, Frost, Adaani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7273341/
https://www.ncbi.nlm.nih.gov/pubmed/32547734
http://dx.doi.org/10.1177/2045894020931315

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7273341/
https://www.ncbi.nlm.nih.gov/pubmed/32547734
http://dx.doi.org/10.1177/2045894020931315

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