The role of oxidative stress in Rett syndrome: an overview
The main cause of Rett syndrome (RTT), a pervasive development disorder almost exclusively affecting females, is a mutation in the methyl‐CpG binding protein 2 (MeCP2) gene. To date, no cure for RTT exists, although disease reversibility has been demonstrated in animal models. Emerging evidence from...
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Published in | Annals of the New York Academy of Sciences Vol. 1259; no. 1; pp. 121 - 135 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Malden, USA
Blackwell Publishing Inc
01.07.2012
Wiley Subscription Services, Inc Wiley |
Subjects | |
Online Access | Get full text |
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