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