Impaired platelet activation in patients with hereditary deficiency of p47phox

Impaired platelet activation in patients with hereditary deficiency of p47^phox

Br J Haematol. 2018 Feb;180(3):454-456. doi: 10.1111/bjh.14347. Epub 2016 Oct 10.

¹ Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Latina, Italy.
² Department of Internal Medicine and Medical Specialties, Sapienza University of Rome, Rome, Italy.
³ Department of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
⁴ Department of Internal Medicine, University of Rome "Tor Vergata", Rome, Italy.
⁵ Department of Pediatrics and Institute of Molecular Medicine "A. Nocivelli", University of Brescia, Brescia, Italy.
⁶ Department of Pediatrics, University of Florence, Florence, Italy.
⁷ Department of Biomedicine and Evolutive Aging, University of Bari, Bari, Italy.
⁸ Department of Pediatrics, University of Naples, Naples, Italy.

No abstract available

Keywords: Nox2; chronic granulomatous disease; oxidative stress; p47phox; platelet activation.