Genetic analysis of Indian subjects with clinical features of possible type IIa hypercholesterolemia-Reference-Cited by-同舟云学术

Genetic analysis of Indian subjects with clinical features of possible type IIa hypercholesterolemia

Published:2007 Issue:6 Volume:21 Page:375-381
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J. Clin. Lab. Anal.

Author:

Kondkar Altaf A.,Nair Kappiareth G.,Ashavaid Tester F.

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry, medical,Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Reference31 articles.

1. Molecular genetics of the LDL receptor gene in familial hypercholesterolemia

2. Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia.

3. Apolipoprotein E: an important gene and protein to follow in laboratory medicine

4. Common Variants in the Promoter of the Hepatic Lipase Gene Are Associated With Lower Levels of Hepatic Lipase Activity, Buoyant LDL, and Higher HDL 2 Cholesterol

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