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 language | English |
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Pages (from-to) | 342-343 |
Number of pages | 2 |
Journal | Nature neuroscience |
Volume | 4 |
Issue number | 4 |
DOIs | |
State | Published - 2001 |