reference/3797234

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publicationName	Haemophilia : the official journal of the World Federation of Hemophilia
startingPage	966
bibliographicCitation	Enayat MS, Guilliatt AM, Short PE, Rastegar-Lari G, Jazebi M, Ravonbod S, Ala F, Chapman OG, Hill FG. A novel alanine or threonine 789 to proline mutation causing type 2N von Willebrand's disease when inherited homozygously or heterozygously with arginine 854 to glutamine mutation. Haemophilia. 2010 Nov;16(6):966–9. doi: 10.1111/j.1365-2516.2010.02271.x. PMID: 20491956.
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date	2010-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/20491956 https://doi.org/10.1111/j.1365-2516.2010.02271.x
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	A novel alanine or threonine 789 to proline mutation causing type 2N von Willebrand’s disease when inherited homozygously or heterozygously with arginine 854 to glutamine mutation
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