Expression of the Familial Hypercholesterolemia Gene in Heterozygotes: Mechanism for a Dominant Disorder in Man
Author:
Affiliation:
1. Department of Internal Medicine, University of Texas Southwestern Medical School. Dallas 75235
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference14 articles.
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2. BROWN, M.S., REGULATION OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME A REDUCTASE-ACTIVITY IN CULTURED HUMAN FIBROBLASTS - COMPARISON OF CELLS FROM A NORMAL SUBJECT AND FROM A PATIENT WITH HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA, JOURNAL OF BIOLOGICAL CHEMISTRY 249: 789 (1974).
3. BROWN, M.S., REGULATION OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME A REDUCTASE-ACTIVITY IN HUMAN FIBROBLASTS BY LIPOPROTEINS, PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 70: 2162 (1973).
4. BROWN, M.S., FAMILIAL HYPERCHOLESTEROLEMIA - DEFECTIVE BINDING OF LIPOPROTEINS TO CULTURED FIBROBLASTS ASSOCIATED WITH IMPAIRED REGULATION OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME A REDUCTASE-ACTIVITY, PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 71: 788 (1974).
5. Kirkman, H. N., Congenital Malformations: 209 (1969).
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