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Publikováno v:
Pulmonary Circulation, Vol 8 (2018)
Despite the discovery more than 15 years ago that patients with hereditary pulmonary arterial hypertension (HPAH) inherit BMP type 2 receptor ( BMPR2 ) mutations, it is still unclear how these mutations cause disease. In part, this is attributable to
Externí odkaz:
https://doaj.org/article/046b38562c854e5cb3d1d1dff47404f6
Autor:
Zeke Buskirk, Peter Knappett, M. Bayani Cardenas, Saugata Datta, Harshad Kulkarni, Tom Varner, Alexander Pappas, Allison Prewitt
Publikováno v:
Goldschmidt2022 abstracts.