DNA deletions in the low density lipoprotein (LDL) receptor gene in Danish families with familial hypercholesterolemia
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1991.tb03057.x/fullpdf
Reference36 articles.
1. Identification of a deletion in the LDL receptor gene: a Finnish type of mutation;Aalto-Setälä;FEBS Lett.,1988
2. Screening for hyperlipoproteinemia in 10000 Danish newborns;Andersen;Acda Padiatr. Scand.,1979
3. The J. D. mutation in familial hypercholesterolemia: amino acid substitution in cytoplasmic domain impedes internalization of LDL receptors;Davis;Cell,1986
4. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity;Feinberg;Anal. Biochem.,1983
5. Estimation of the concentration of the low density lipoprotein cholesterol in plasma without use of the preparative ultracentrifuge;Friedenwald;Clin. Chem.,1972
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