Genetic diagnosis of familial hypercholesterolaemia using a rapid biochip array assay for 40 common LDLR, APOB and PCSK9 mutations
Autor: | Martin, Rosalind, Latten, Mark, Hart, Padraig, Murray, Helena, Bailie, Deborah A., Crockard, Martin, Lamont, John, Fitzgerald, Peter, Graham, Colin A. |
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Zdroj: | In Atherosclerosis November 2016 254:8-13 |
Databáze: | ScienceDirect |
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