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Lecithin cholesterol acyltransferase deficiency : ウィキペディア英語版 | Lecithin cholesterol acyltransferase deficiency
Lecithin cholesterol acyltransferase deficiency (LCAT deficiency) is disorder of lipoprotein metabolism. Lecithin cholesterol acyltransferase catalyzes the formation of cholesterol esters in lipoproteins. ==Types== The disease has two forms: * familial LCAT deficiency in which there is complete LCAT deficiency. * fish eye disease in which there is a partial deficiency. Both are autosomal recessive disorders caused by mutations of the ''LCAT'' gene located on chromosome 16q22.
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Lecithin cholesterol acyltransferase deficiency」の詳細全文を読む
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