Defective Apolipoprotein B-100
Last Posted: Nov 05, 2013
- Decreased bone mineral density in subjects carrying familial defective apolipoprotein B-100.
Yerges-Armstrong Laura M, et al. The Journal of clinical endocrinology and metabolism 2013 12 (12) E1999-2005
- Molecular description of familial defective APOB-100 in Malaysia.
Al-Khateeb Alyaa R, et al. Biochemical genetics 2013 10 (9-10) 811-23
- Defective apolipoprotein B-100
From NCATS Genetic and Rare Diseases Information Center
- Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish.
Shen Haiqing, et al. Archives of internal medicine 2010 11 (20) 1850-5
- Lipid levels and their genetic regulation in patients with familial hypercholesterolemia and familial defective apolipoprotein B-100: the MEDPED Slovakia Project.
Vohnout Branislav, et al. Atherosclerosis. Supplements 2003 11 (3) 3-5
- Apolipoprotein B Arg3500Gln mutation prevalence in children with hypercholesterolemia: a French multicenter study.
Viola S, et al. Journal of pediatric gastroenterology and nutrition 2001 8 (2) 122-6
- Effect of apolipoprotein E polymorphism and apolipoprotein A-1 gene promoter polymorphism on lipid parameters and premature coronary artery disease.
Petrovic D, et al. Folia biologica 2000 0 (5) 181-5
- Familial defective apolipoprotein B-100 in a group of hypercholesterolaemic patients in Poland. Identification of a new mutation Thr3492Ile in the apolipoprotein B gene.
Bednarska-Makaruk M, et al. European journal of human genetics : EJHG 2001 11 (11) 836-42
- Low-density lipoprotein receptor gene mutation analysis and clinical correlation in Belgian hypercholesterolaemics.
Van Gaal L F, et al. Molecular and cellular probes 2001 12 (6) 329-36
- The apolipoprotein B R3500Q gene mutation in Spanish subjects with a clinical diagnosis of familial hypercholesterolemia.
Castillo Sergio, et al. Atherosclerosis 2002 11 (1) 127-35
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