🚨🚨Another New preprint from the lab🚨🚨
MeCP2 is a key regulator of gene silencing. Over 800 different mutations in the X-linked MECP2 gene are known to cause Rett Syndrome. We ask how MeCP2 engages with nucleosomes & how variants affect engagement with chromatin.
www.biorxiv.org/content/10.6...
