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Showing results (21-30 of 23) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|May 1, 1990
Lipoprotein lipaseBethesda: a single amino acid substitution (Ala-176----Thr) leads to abnormal heparin binding and loss of enzymic activityO U Beg, M S Meng, S I Skarlatos, et al.
The Journal of Biological Chemistry|January 15, 1991
Identification of two separate allelic mutations in the lipoprotein lipase gene of a patient with the familial hyperchylomicronemia syndromeH L Dichek, S S Fojo, O U Beg, et al.
Journal of Lipid Research|March 1, 1996
Homozygosity for two point mutations in the lipoprotein lipase (LPL) gene in a patient with familial LPL deficiency: LPL(Asp9-->Asn, Tyr262-->His)M Rouis, P Lohse, K A Dugi, et al.
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Showing results (21-30 of 23) with videos related to

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Pageof 3
You have reached the last page of results.This site can display upto 23 results.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1990
Lipoprotein lipaseBethesda: a single amino acid substitution (Ala-176----Thr) leads to abnormal heparin binding and loss of enzymic activityO U Beg, M S Meng, S I Skarlatos, et al.
The Journal of Biological Chemistry|January 15, 1991
Identification of two separate allelic mutations in the lipoprotein lipase gene of a patient with the familial hyperchylomicronemia syndromeH L Dichek, S S Fojo, O U Beg, et al.
Journal of Lipid Research|March 1, 1996
Homozygosity for two point mutations in the lipoprotein lipase (LPL) gene in a patient with familial LPL deficiency: LPL(Asp9-->Asn, Tyr262-->His)M Rouis, P Lohse, K A Dugi, et al.
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