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MeCP2 functions largely cell-autonomously, but also non-cell-autonomously, in neuronal maturation and dendritic arborization of cortical pyramidal neurons

Rett syndrome is a human neurodevelopmental disorder presenting almost exclusively in female infants; it is the second most common cause of mental retardation in girls, after Down’s syndrome. The identification in 1999 that mutation of the methyl-CpG-binding protein 2 (MECP2) gene on the X chromosom...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Kishi, Noriyuki, Macklis, Jeffrey D.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2009
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2846301/
https://ncbi.nlm.nih.gov/pubmed/20025874
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.expneurol.2009.12.007
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