FOXG1 Regulates PRKAR2B Transcriptionally and Posttranscriptionally via miR200 in the Adult Hippocampus
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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… read more here.
Keywords: transcriptionally posttranscriptionally; foxg1 regulates; prkar2b transcriptionally; posttranscriptionally via ... See more keywords