JASReference:Bujo H:Kusunoki J:Ogasawara M:Yamamoto T:Ohta Y:Shimada T:Saito Y:Yoshida S:,Biochem Biophys Res Commun,1991,181,933: Difference between revisions
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{{JASReference|mutation= | {{JASReference|mutation= | ||
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|title=Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease | |title=Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease | ||
|doi=10.1016/0006-291X(91)92026-G | |doi=10.1016/0006-291X(91)92026-G | ||
|pmid=1662503 | |pmid=1662503 | ||
}} | }} | ||
Revision as of 11:25, 20 July 2012
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| Title | Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease |
| Author(s) | (Click a name to see records for each author.) |
| Journal | Biochemical and Biophysical Research Communications (8 pages) |
| Year | 1991 |
| Volume | 181 |
| Page | 933 |
Genetic mutations in this article
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How to input/edit information?
- Account Information
This database is maintained by the subcommittee for Lipid Metabolism in Japan Atherosclerosis Society. If you volunteer to contribute, please contact arita AT k.u-tokyo.ac.jp. |
このデータベースは日本動脈硬化学会 脂質代謝部会が作成しています。入力等に協力していただける方は有田 arita AT k.u-tokyo.ac.jp までご連絡下さい。 |
- Format of the page
The format of the page title is here. The format of mutation information is here. |
