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[Apolipoprotein C-II deficiency].
Nihon rinsho. Japanese journal of clinical medicine, 1995Apo C-II has a central role in triglyceride metabolism as a cofactor for lipoprotein lipase (LPL), the enzyme that catalyzes the hydrolysis of triglycerides on plasma lipoproteins. Apo C-II deficiency is a rare genetic disorder that is inherited as an autosomal recessive trait.
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Apolipoprotein A-II: beyond genetic associations with lipid disorders and insulin resistance
Current Opinion in Lipidology, 2003A. Kalopissis, D. Pastier, J. Chambaz
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Immunochemistry of human plasma high density lipoproteins. Radioimmunoassay of apolipoprotein A-II
, 1975S. Mao, A. Gotto, R. Jackson
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[Apolipoprotein A-II abnormality].
Ryoikibetsu shokogun shirizu, 1998S, Takahashi, I, Miyamori
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Biochimica et Biophysica Acta, 1987
B. Fong, A. Salter, J. Jimenez, A. Angel
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B. Fong, A. Salter, J. Jimenez, A. Angel
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Apolipoprotein C-II deficiency
Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1984W. Haberbosch +5 more
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