LAUSR

IGF1 neuronal response in the absence of MECP2 is dependent on TRalpha 3

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1 Published in 2017 at "Human Molecular Genetics"

DOI: 10.1093/hmg/ddw384

Abstract: Rett syndrome (RTT) is an X-linked neurodevelopmental disorder in which the MECP2 (methyl CpG-binding protein 2) gene is mutated. Recent studies showed that RTT-derived neurons have many cellular deficits when compared to control, such as:… read more here.

Keywords: rtt; igf1 neuronal; derived neurons; mecp2 ... See more keywords