[3P] Late-Breaking Abstracts

[H. Disorders of Nervous Systems] Neurodevelopmental Disorders

[3P-367] Molecular mechanism of CBX1-related syndrome, a neurodevelopmental disorder due to HP1β dysfunction.

*Kosuke Izumi¹, Yukiko Kuroda², Aiko Otsubo², Izumi Kazama², Anita Kabahizi¹, Graciella Carrilo¹, Randy Le¹, Chun Su², Struan Grant² (1. University of Texas Southwestern Medical Center, 2. The Children's Hospital of Philadelphia)

Keywords:

hetrerochromatin,epigenetics,autism,developmental disabilities

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