reference/30165417

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publicationName	Atherosclerosis
startingPage	331
bibliographicCitation	Graham CA, McIlhatton BP, Kirk CW, Beattie ED, Lyttle K, Hart P, Neely RD, Young IS, Nicholls DP. Genetic screening protocol for familial hypercholesterolemia which includes splicing defects gives an improved mutation detection rate. Atherosclerosis. 2005 Oct;182(2):331–40. doi: 10.1016/j.atherosclerosis.2005.02.016. PMID: 16159606.
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date	200510
identifier	https://doi.org/10.1016/j.atherosclerosis.2005.02.016 https://pubmed.ncbi.nlm.nih.gov/16159606
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Genetic screening protocol for familial hypercholesterolemia which includes splicing defects gives an improved mutation detection rate
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