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.
Zdroj: In Atherosclerosis November 2016 254:8-13
Databáze: ScienceDirect