reference/1722437

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1722437

Outgoing Links

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contentType	Letter\|Research Support, Non-U.S. Gov't
endingPage	99
issn	0009-9163 1399-0004
issueIdentifier	1
pageRange	97-99
publicationName	Clinical Genetics
startingPage	97
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bibliographicCitation	Taylor A, Patel K, Tsedeke J, Humphries SE, Norbury G. Mutation screening in patients for familial hypercholesterolaemia (ADH). Clin Genet. 2010 Jan;77(1):97–9. doi: 10.1111/j.1399-0004.2009.01279.x. PMID: 19843101.
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date	2009-12-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1111/j.1399-0004.2009.01279.x https://pubmed.ncbi.nlm.nih.gov/19843101
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Mutation screening in patients for familial hypercholesterolaemia (ADH)
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Total number of triples: 42.