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Mutational analysis of human lipoprotein lipase by carboxy-terminal truncation

We have previously reported a Trp382 (TGG)–>stop (TGA) mutation that causes familial lipoprotein lipase (LPL) deficiency. Expression study of the Trp382–>stop mutant showed that the truncated LPL was catalytically inactive with a marked reduction in the expressed mass. To investigate the minimal ami...

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Principais autores: K Kozaki, T Gotoda, M Kawamura, H Shimano, Y Yazaki, Y Ouchi, H Orimo, N Yamada
Formato: Artigo
Idioma:Inglês
Publicado: Elsevier 1993-10-01
Series:Journal of Lipid Research
Acceso en liña:http://www.sciencedirect.com/science/article/pii/S0022227520357394
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