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Published in 2018 at "Molecular Neurobiology"
DOI: 10.1007/s12035-018-1444-7
Abstract: Rett syndrome is a complex neurodevelopmental disorder that is mainly caused by mutations in MECP2. However, mutations in FOXG1 cause a less frequent form of atypical Rett syndrome, called FOXG1 syndrome. FOXG1 is a key…
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Keywords:
transcriptionally posttranscriptionally;
foxg1 regulates;
prkar2b transcriptionally;
posttranscriptionally via ... See more keywords