Interplay of LIS1 and MeCP2: Interactions and Implications With the Neurodevelopmental Disorders Lissencephaly and Rett Syndrome
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DOI: 10.3389/fncel.2019.00370
Abstract: LIS1 is the main causative gene for lissencephaly, while MeCP2 is the main causative gene for Rett syndrome, both of which are neurodevelopmental diseases. Here we report nuclear functions for LIS1 and identify previously unrecognized… read more here.
Keywords: rett syndrome; mecp2; disorders lissencephaly; lis1 ... See more keywords