Defective assembly of the respiratory chain

被引:1
作者
Esteitie, N
Larsson, NG [1 ]
机构
[1] Karolinska Univ Hosp, Karolinska Inst, Novum, Dept Med Nutr, SE-14186 Stockholm, Sweden
[2] Karolinska Univ Hosp, Karolinska Inst, Novum, Dept Woman & Child Hlth, SE-14186 Stockholm, Sweden
关键词
encephalopathy; cardiomyopathy; mitochondria; cytochrome c oxidase;
D O I
10.1080/08035250410018256
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
A functional respiratory chain is dependent on protein components encoded by both mtDNA and nuclear DNA. Isolated cytochrome c oxidase (COX) deficiency is often caused by mutations in nuclear genes regulating the assembly of the 13 protein subunits of this complex. The accompanying paper by Zeman and co-workers reports that mutations in SCO2 are common in infantile COX deficiency and are associated with a very poor prognosis. Conclusion: Molecular diagnosis is often feasible in patients with COX deficiency and particular attention should be paid to mutations in COX assembly genes.
引用
收藏
页码:1268 / 1270
页数:3
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