Author:
Murano Takeyoshi,Miyashita Yoh,Itoh Yoshiaki,Tsuzuki Satoko,Yamamori Syunji,Watanabe Hitoshi,Shirai Kohji
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference24 articles.
1. Brunzell JD. Familial lipoprotein lipase deficiency and other causes of the chylomicronemia syndrome. In: Serivier CR, Beaudet AL, Sly WS, Valle D, editors. The Metabolic basis of inherited diseases, vol II. 7th. Ed. McGraw-Hill. New York. 1995:1913–32.
2. Lipoprotein lipase. A multifunctional enzyme relevant to common metabolic diseases;Eckel;N Eng J Med.,1989
3. Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia;Gange;Arterioscler. Thromb.,1994
4. The lipoprotein lipase (Asn291-Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidemia;Hoffer;Atherosclerosis.,1996
5. Catalytic triad residue mutation (Asp 156→Gly) causing familial lipoprotein lipase deficiency;Faustinella;J. Biol. Chem.,1991
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