Schon E A
Depts of Neurology and of Genetics and Development, Columbia University, New York, NY 10032, USA.
Trends Biochem Sci. 2000 Nov;25(11):555-60. doi: 10.1016/s0968-0004(00)01688-1.
Mitochondrial respiratory chain diseases are a highly diverse group of disorders whose main unifying characteristic is the impairment of mitochondrial function. As befits an organelle containing gene products encoded by both mitochondrial DNA (mtDNA) and nuclear DNA (nDNA), these diseases can be caused by inherited errors in either genome, but a surprising number are sporadic, and a few are even caused by environmental factors.
线粒体呼吸链疾病是一组高度多样化的疾病,其主要的共同特征是线粒体功能受损。作为一个包含由线粒体DNA(mtDNA)和核DNA(nDNA)编码的基因产物的细胞器,这些疾病可能由任一基因组中的遗传错误引起,但令人惊讶的是,有相当数量的病例是散发性的,甚至有一些是由环境因素引起的。