THE ENZYMES OF MITOCHONDRIAL FATTY-ACID OXIDATION

被引：10
作者：
BENNETT, MJ
机构：
[1] Department of Pathology. University, Texas Southwestern Medical Center, Children's Medical Center of Dallas, Dallas, TX 75235
来源：
CLINICA CHIMICA ACTA | 1994年 / 226卷 / 02期
关键词：
INHERITED METABOLIC DISEASES; SCREENING; ENERGY METABOLISM; BETA-OXIDATION;
D O I：
10.1016/0009-8981(94)90216-X
中图分类号：
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号：
1001 ;
摘要：
Defects of mitochondrial fatty acid oxidation are recent additions to the catalogue of inherited metabolic diseases. This review focuses upon decent developments in our understanding of the basic biochemistry, clinical presentations and molecular genetics of fatty acid oxidation disorders, with an emphasis on the strategies being used to define new disorders.
引用
收藏
页码：211 / 224
页数：14
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