Rett syndrome model suggests MECP2 gives neurons the quiet they need to think

A. R. Carter, R. A. Segal

Research output: Contribution to journalShort survey

6 Scopus citations

Abstract

The neurodevelopmental disorder Rett syndrome involves mutations in the transcriptional repressor MECP2. Two groups now show a role for MECP2 in postmitotic mouse neurons.

Original languageEnglish
Pages (from-to)342-343
Number of pages2
JournalNature neuroscience
Volume4
Issue number4
DOIs
StatePublished - Apr 12 2001
Externally publishedYes

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