Genetics and Genomics of Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is a rare disorder that may be hereditable (HPAH), idiopathic (IPAH), or associated with either drug-toxin exposures or other medical conditions. Familial cases have long been recognised and are usually due to mutations in Bone Morphogenetic Protein Receptor typ...

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Bibliografiset tiedot
Päätekijät: Machado, Rajiv D., Eickelberg, Oliver, Elliott, Greg, Geraci, Mark W., Hanaoka, Masayuki, Loyd, James E., Newman, John H., Phillips, John A., Soubrier, Florent, Trembath, Richard C., Chung, Wendy K.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2009
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3725550/
https://ncbi.nlm.nih.gov/pubmed/19555857
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jacc.2009.04.015
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