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Angelman Syndrome
Angelman syndrome is a neurogenetic imprinting disorder caused by loss of the maternally inherited UBE3A gene and is characterized by generalized epilepsy, limited expressive speech, sleep dysfunction, and movement disorders. Here is the latest research.
Related Papers
Angelman syndrome scientific symposium on the structure and function of UBE3A/E6AP
(opens in new tab)Journal of Child Neurology
Charles A Williams
Current Opinion in Genetics & Development
Y H JiangA L Beaudet
Neurobiology of Disease
Kiyonori MiuraJ Wagstaff
Journal of Neurodevelopmental Disorders
Benjamin D PhilpotCharles A Williams
Activity-dependent changes in MAPK activation in the Angelman Syndrome mouse model
(opens in new tab)Learning & Memory
Irina FilonovaEdwin J Weeber