Wanders Ronald J A
University of Amsterdam, Academic Medical Centre, Department of Clinical Chemistry, Emma Children's Hospital, Laboratory of Genetic Metabolic Diseases, Amsterdam, The Netherlands.
Am J Med Genet A. 2004 May 1;126A(4):355-75. doi: 10.1002/ajmg.a.20661.
The group of peroxisomal disorders now includes 17 different disorders with Zellweger syndrome as prototype. Thanks to the explosion of new information about the functions and biogenesis of peroxisomes, the metabolic and molecular basis of most of the peroxisomal disorders has been resolved. A review of peroxisomal disorders is provided in this paper.
现在，过氧化物酶体疾病组包括以泽尔韦格综合征为原型的17种不同疾病。由于有关过氧化物酶体功能和生物发生的新信息激增，大多数过氧化物酶体疾病的代谢和分子基础已得到解决。本文对过氧化物酶体疾病进行了综述。
