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Hyperlipoproteinaemia(a) is a common cause of autosomal dominant hypercholesterolaemia.
Meriño-Ibarra E, Puzo J, Jarauta E, Cenarro A, Recalde D, García-Otín AL, Ros E, Martorell E, Pintó X, Franco M, Zambón D, Brea A, Pocoví M, Civeira F. Meriño-Ibarra E, et al. Among authors: recalde d. J Inherit Metab Dis. 2007 Nov;30(6):970-7. doi: 10.1007/s10545-007-0585-z. Epub 2007 Oct 20. J Inherit Metab Dis. 2007. PMID: 17955342
A novel DNA polymorphism (4886C>T) in the human LCAT gene.
Recalde D, Cenarro A, Civeira F, Garcia-Otin AL, Pocovi M. Recalde D, et al. Hum Mutat. 2000 Mar;15(3):298. doi: 10.1002/(SICI)1098-1004(200003)15:3<298::AID-HUMU21>3.0.CO;2-A. Hum Mutat. 2000. PMID: 10679956 No abstract available.
Allelic polymorphism -491A/T in apo E gene modulates the lipid-lowering response in combined hyperlipidemia treatment.
García-Otín AL, Civeira F, Aristegui R, Díaz C, Recalde D, Sol JM, Masramon X, Hernández G, Pocoví M; ATOMIX Study Group. Atorvastatin in Mixed dyslipidemia. García-Otín AL, et al. Among authors: recalde d. Eur J Clin Invest. 2002 Jun;32(6):421-8. doi: 10.1046/j.1365-2362.2002.00996.x. Eur J Clin Invest. 2002. PMID: 12059987 Clinical Trial.
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