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T-1131-->C polymorphism within the apolipoprotein AV gene in hypertriglyceridemic individuals.
PMID: 12818421 [PubMed - indexed for MEDLINE]
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Cited by 4 PubMed Central articles
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Triglyceride associated polymorphisms of the APOA5 gene have very different allele frequencies in Pune, India compared to Europeans.
Chandak GR, Ward KJ, Yajnik CS, Pandit AN, Bavdekar A, Joglekar CV, Fall CH, Mohankrishna P, Wilkin TJ, Metcalf BS, et al.
BMC Med Genet. 2006 Oct 10; 7:76. Epub 2006 Oct 10.
[BMC Med Genet. 2006]
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Allelic drop-out may occur with a primer binding site polymorphism for the commonly used RFLP assay for the -1131T>C polymorphism of the Apolipoprotein AV gene.
Ward KJ, Ellard S, Yajnik CS, Frayling TM, Hattersley AT, Venigalla PN, Chandak GR.
Lipids Health Dis. 2006 May 2; 5:11. Epub 2006 May 2.
[Lipids Health Dis. 2006]
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Apoa5 Q139X truncation predisposes to late-onset hyperchylomicronemia due to lipoprotein lipase impairment.
Marçais C, Verges B, Charrière S, Pruneta V, Merlin M, Billon S, Perrot L, Drai J, Sassolas A, Pennacchio LA, et al.
J Clin Invest. 2005 Oct; 115(10):2862-9.
[J Clin Invest. 2005]
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