reference/24097929

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/24097929

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startingPage	2671
bibliographicCitation	Martinez-Duncker I, Dupré T, Piller V, Piller F, Candelier JJ, Trichet C, Tchernia G, Oriol R, Mollicone R. Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter. Blood. 2005 Apr 01;105(7):2671–6. doi: 10.1182/blood-2004-09-3509. PMID: 15576474.
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date	2005-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1182/blood-2004-09-3509 https://pubmed.ncbi.nlm.nih.gov/15576474
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter
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