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Proceedings of the National Academy of Sciences of the United States of America|June 1, 1991
A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activityH Funke, A von Eckardstein, P H Pritchard, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 1, 1995
Electrophoretic screening for human apolipoprotein C-II variants: repeated identification of apolipoprotein C-II(K19T)H Wiebusch, J R Nofer, A von Eckardstein, et al.
Zeitschrift Fur Kardiologie|May 16, 2000
Molecular genetics of arrhythmias--a new paradigmE Schulze-Bahr, W Haverkamp, M Borggrefe, et al.
Human Genetics|October 28, 1997
Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneousE Schulze-Bahr, W Haverkamp, H Wedekind, et al.
Journal of Molecular Medicine (Berlin, Germany)|November 1, 1995
Molecular analysis at the Harvey Ras-1 gene in patients with long QT syndromeE Schulze-Bahr, W Haverkamp, H Wiebusch, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 1, 1995
A novel variant of lysosomal acid lipase (Leu336-->Pro) associated with acid lipase deficiency and cholesterol ester storage diseaseU Seedorf, H Wiebusch, S Muntoni, et al.
Current Opinion in Lipidology|June 1, 1997
Genetic determinants of high density lipoprotein levelsH Funke
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