CDKL5 mutation is associated with an atypical Rett syndrome (RTT) variant. Recently, cholesterol homeostasis perturbation and oxidative-mediated loss of the high-density lipoprotein receptor SRB1 in typical RTT have been suggested. Here, we demonstrate an altered lipid serum profile also in CDKL5 patients with decreased levels of SRB1 and impaired… (More)
The Publisher regrets that this article is an accidental duplication of an article that has already been published, 10.1016/j.freeradbiomed.2013.09.018. The duplicate article has therefore been withdrawn.