reference/26882481

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/26882481

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endingPage	434
issn	1079-5642 1524-4636
issueIdentifier	2
pageRange	423-434
publicationName	Arteriosclerosis, Thrombosis, and Vascular Biology
startingPage	423
bibliographicCitation	Pignatelli P, Carnevale R, Di Santo S, Bartimoccia S, Sanguigni V, Lenti L, Finocchi A, Mendolicchio L, Soresina AR, Plebani A, Violi F. Inherited human gp91phox deficiency is associated with impaired isoprostane formation and platelet dysfunction. Arterioscler Thromb Vasc Biol. 2011 Feb;31(2):423–34. doi: 10.1161/atvbaha.110.217885. PMID: 21071703.
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date	201102
identifier	https://pubmed.ncbi.nlm.nih.gov/21071703 https://doi.org/10.1161/atvbaha.110.217885
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Inherited Human gp91 phox Deficiency Is Associated With Impaired Isoprostane Formation and Platelet Dysfunction
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