reference/2596340

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/2596340

Outgoing Links

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contentType	Journal Article\|Multicenter Study
endingPage	41
issn	0957-5235
issueIdentifier	1
pageRange	34-41
publicationName	Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
startingPage	34
bibliographicCitation	Mitchell M, Gattens M, Kavakli K, Liesner R, Payne J, Norton M, Austin S. Genotype analysis and identification of novel mutations in a multicentre cohort of patients with hereditary factor X deficiency. Blood Coagul Fibrinolysis. 2019 Jan;30(1):34–41. doi: 10.1097/mbc.0000000000000787. PMID: 30507709.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_45075c3874699c3b09c42b09a7215040 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_b1b650ae4b42c77cced80bc8253eb651 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_c9975f298e4256bd3f68d1f808423a0f http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_063182b7d3eb49afe20205167d497977 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_36f26a4f397b2c7317f289f6223d9208 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_63eb923f77c2732ff302394d4daf7cb7 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_550e1cb6856dd8da221654e7aa6e9383
date	201901
identifier	https://doi.org/10.1097/mbc.0000000000000787 https://pubmed.ncbi.nlm.nih.gov/30507709
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/1165 https://portal.issn.org/resource/ISSN/0957-5235
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Genotype analysis and identification of novel mutations in a multicentre cohort of patients with hereditary factor X deficiency
discusses	http://id.nlm.nih.gov/mesh/M0008154
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Incoming Links

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isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID2159

Total number of triples: 40.