Combined Lipase Deficiency ( cld ): a Lethal Mutation on Chromosome 17 of the Mouse
Author:
Affiliation:
1. Division of Arteriosclerosis and Metabolism, Mount Sinai School of Medicine, New York 10029
2. Section of Developmental Genetics, Sloan-Kettering Institute, New York 10021
Publisher
American Association for the Advancement of Science (AAAS)
Subject
Multidisciplinary
Reference26 articles.
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2. AUGUSTIN, J, ATHEROSCLEROSIS REVIEWS 5: 91 (1979).
3. AUGUSTIN, J, COMPARISON OF MOLECULAR-PROPERTIES OF HEPATIC TRIGLYCERIDE LIPASE AND LIPOPROTEIN-LIPASE FROM HUMAN POST-HEPARIN PLASMA, JOURNAL OF BIOLOGICAL CHEMISTRY 253: 2912 (1978).
4. BABIARZ, B, GENETIC-ANALYSIS OF THE TW73 HAPLOTYPE OF THE MOUSE USING DELETION MUTATIONS - EVIDENCE FOR A PARASITIC LETHAL MUTATION, GENETICAL RESEARCH 39: 111 (1982).
5. BAGINSKY, M.L., NEW METHOD FOR THE MEASUREMENT OF LIPOPROTEIN-LIPASE IN POST-HEPARIN PLASMA USING SODIUM DODECYL-SULFATE FOR THE INACTIVATION OF HEPATIC TRIGLYCERIDE LIPASE, JOURNAL OF LIPID RESEARCH 20: 548 (1979).
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