Increased levels of 4HNE-protein plasma adducts in Rett syndrome.

Abstract

OBJECTIVE Rett syndrome (RTT) is a neurological disorder and a leading cause of mental retardation in females. It is caused by mutations in methyl-CpG-binding protein 2 (MeCP2) gene and more rarely in cyclin-dependent kinase-like 5 (CDKL5) and forkhead box protein G1 (FOXG1) genes. Increased oxidative stress (OS) has been documented in MeCP2-RTT patients… (More)
DOI: 10.1016/j.clinbiochem.2011.01.007

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Cite this paper

@article{Pecorelli2011IncreasedLO, title={Increased levels of 4HNE-protein plasma adducts in Rett syndrome.}, author={Alessandra Pecorelli and L. 12 Cohen Ciccoli and Cinzia Signorini and Silvia Leoncini and Anna Giardini and Maurizio D'Esposito and Stefania Filosa and Joussef Hayek and Claudio De Felice and Giuseppe Valacchi}, journal={Clinical biochemistry}, year={2011}, volume={44 5-6}, pages={368-71} }