reference/32747559

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/32747559

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endingPage	2979
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bibliographicCitation	Bodó I, Katsumi A, Tuley EA, Eikenboom JC, Dong Z, Sadler JE. Type 1 von Willebrand disease mutation Cys1149Arg causes intracellular retention and degradation of heterodimers: a possible general mechanism for dominant mutations of oligomeric proteins. Blood. 2001 Nov 15;98(10):2973–9. doi: 10.1182/blood.v98.10.2973. PMID: 11698279.
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date	2001-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1182/blood.v98.10.2973 https://pubmed.ncbi.nlm.nih.gov/11698279
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Type 1 von Willebrand disease mutation Cys1149Arg causes intracellular retention and degradation of heterodimers: a possible general mechanism for dominant mutations of oligomeric proteins
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