Familial Defective Apolipoprotein B-100: A Study of Patients from Lipid Clinics in Scotland and Wales
Author:
Affiliation:
1. Cardiology Department, The Royal Infirmary, Edinburgh EH3 9YW
2. Department of Chemical Pathology, Royal Gwent Hospital, Newport, Gwent NP9 2UB
3. Department of Clinical Biochemistry, The Royal Infirmary, Edinburgh EH3 9YW, UK
Abstract
Publisher
SAGE Publications
Subject
Clinical Biochemistry,General Medicine
Link
http://journals.sagepub.com/doi/pdf/10.1177/000456329603300508
Reference30 articles.
1. A Receptor-Mediated Pathway for Cholesterol Homeostasis
2. Familial defective apolipoprotein B-100: a single mutation that causes hypercholesterolemia and premature coronary artery disease
3. Familial defective apolipoprotein B-100: a review, including some comparisons with familial hypercholesterolaemia
4. Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100.
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2. Comparison of apolipoprotein B metabolism in familial defective apolipoprotein B and heterogeneous familial hypercholesterolemia;Atherosclerosis;2002-05
3. High frequency of the ApoB-100 R3500Q mutation in Bulgarian hypercholesterolaemic subjects;Journal of Medical Genetics;2001-08-01
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