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Multiplex ligation-dependent probe amplification analysis to screen for deletions and duplications of the LDLR gene in patients with familial hypercholesterolaemia

Taylor, A; Martin, B; Wang, D; Patel, K; Humphries, SE; Norbury, G; (2009) Multiplex ligation-dependent probe amplification analysis to screen for deletions and duplications of the LDLR gene in patients with familial hypercholesterolaemia. CLINICAL GENETICS , 76 (1) pp. 69-75. 10.1111/j.1399-0004.2009.01168.x.

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Type: Article
Title: Multiplex ligation-dependent probe amplification analysis to screen for deletions and duplications of the LDLR gene in patients with familial hypercholesterolaemia
DOI: 10.1111/j.1399-0004.2009.01168.x
Keywords: Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, GENETICS & HEREDITY, APOB, autosomal dominant hypercholesterolaemia, familial hypercholesterolaemia, low-density lipoprotein receptor, multiplex ligation-dependent probe amplification analysis, PCSK9, LIPOPROTEIN RECEPTOR GENE, UNITED-KINGDOM, MUTATIONS, IDENTIFICATION, DIAGNOSIS, DISEASE, MLPA, DNA
UCL classification: UCL > School of Life and Medical Sciences
UCL > School of Life and Medical Sciences > Faculty of Population Health Sciences > Institute of Cardiovascular Science
URI: http://discovery.ucl.ac.uk/id/eprint/137981
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