Detection of a new compound heterozygote (del G916/G1401A) for lipoprotein lipase deficiency and a comparative haplotype analysis of the mutant lipoprotein lipase gene from Japanese patients-Reference-Cited by-同舟云学术

Detection of a new compound heterozygote (del G916/G1401A) for lipoprotein lipase deficiency and a comparative haplotype analysis of the mutant lipoprotein lipase gene from Japanese patients

Published:1999-06 Issue:2 Volume:144 Page:443-447
ISSN:0021-9150
Container-title:Atherosclerosis
language:en
Short-container-title:Atherosclerosis

Author:

Okubo Minoru,Inoue Shigeaki,Horinishi Asako,Ogihara Takeshi,Kaneko Ken-ichiro,Gotoda Takanari,Yamada Nobuhiro,Murase Toshio

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference16 articles.

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3. A sandwich-enzyme immunoassay for the quantification of lipoprotein lipase and hepatic triglyceride lipase in human postheparin plasma using monoclonal antibodies to the corresponding enzymes;Ikeda;J. Lipid. Res.,1990

4. Heterogeneous mutations in the human lipoprotein lipase gene in patients with familial lipoprotein lipase deficiency;Gotoda;J. Clin. Invest.,1991

5. A newly identified null allelic mutation in the human lipoprotein lipase (LPL) gene of a compound heterozygote with familial LPL deficiency;Gotoda;Biochim. Biophys. Acta.,1992

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