reference/1067714

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1067714

Outgoing Links

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contentType	Journal Article
endingPage	234
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pageRange	230-234
publicationName	Thrombosis Research
startingPage	230
bibliographicCitation	Tjeldhorn L, Sandset PM, Haugbro K, Skretting G. Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis. Thromb Res. 2010 Mar;125(3):230–4. doi: 10.1016/j.thromres.2009.05.013. PMID: 19535131.
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date	201003
identifier	https://doi.org/10.1016/j.thromres.2009.05.013 https://pubmed.ncbi.nlm.nih.gov/19535131
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Hereditary protein C deficiency caused by the Ala267Thr mutation in the protein C gene is associated with symptomatic and asymptomatic venous thrombosis
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Total number of triples: 48.