Angelman syndrome is a neurodevelopmental disorder caused by mutations in the maternally inherited UBE3A gene, which encodes a ubiquitin ligase. Greer et al. (2010) now identify a UBE3A substrate called Arc that promotes endocytosis of neuronal AMPA receptors, providing insight into synaptic defects that may underlie the cognitive deficits in Angelman syndrome
In this review we summarize the clinical and genetic aspects of Angelman syndrome (AS), its molecula...
"Angelman syndrome" (AS) is a neurodevelopmental disorder whose main features are intellectual disab...
Angelman syndrome is a neurogenetic disorder characterized by developmental delay, severe intellectu...
Angelman syndrome is a neurodevelopmental disorder caused by mutations in the maternally inherited U...
the neuroscience of UBE3A. Angelman syndrome is characterized by loss of speech, severe developmenta...
SummaryAngelman Syndrome is a debilitating neurological disorder caused by mutation of the E3 ubiqui...
Angelman Syndrome is a debilitating neurological disorder caused by mutation of the E3 ubiquitin lig...
Angelman Syndrome is a debilitating neurological disorder caused by mutation of the E3 ubiquitin lig...
Angelman syndrome is a neurodevelopmental disorder caused by mutations in the maternally inherited U...
Angelman syndrome is a severe neurodevelopmental disorder caused by mutations in UBE3A. Sun et al. (...
SummaryAngelman Syndrome is a debilitating neurological disorder caused by mutation of the E3 ubiqui...
Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by mutation or deletion of the...
This review briefly discusses key recent research literature on Angelman Syndrome (AS), a rare genet...
This report is a meeting summary of the 2010 Angelman Syndrome Foundation's scientific symposium on ...
This report is a meeting summary of the 2010 Angelman Syndrome Foundation's scientific symposium on ...
In this review we summarize the clinical and genetic aspects of Angelman syndrome (AS), its molecula...
"Angelman syndrome" (AS) is a neurodevelopmental disorder whose main features are intellectual disab...
Angelman syndrome is a neurogenetic disorder characterized by developmental delay, severe intellectu...
Angelman syndrome is a neurodevelopmental disorder caused by mutations in the maternally inherited U...
the neuroscience of UBE3A. Angelman syndrome is characterized by loss of speech, severe developmenta...
SummaryAngelman Syndrome is a debilitating neurological disorder caused by mutation of the E3 ubiqui...
Angelman Syndrome is a debilitating neurological disorder caused by mutation of the E3 ubiquitin lig...
Angelman Syndrome is a debilitating neurological disorder caused by mutation of the E3 ubiquitin lig...
Angelman syndrome is a neurodevelopmental disorder caused by mutations in the maternally inherited U...
Angelman syndrome is a severe neurodevelopmental disorder caused by mutations in UBE3A. Sun et al. (...
SummaryAngelman Syndrome is a debilitating neurological disorder caused by mutation of the E3 ubiqui...
Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by mutation or deletion of the...
This review briefly discusses key recent research literature on Angelman Syndrome (AS), a rare genet...
This report is a meeting summary of the 2010 Angelman Syndrome Foundation's scientific symposium on ...
This report is a meeting summary of the 2010 Angelman Syndrome Foundation's scientific symposium on ...
In this review we summarize the clinical and genetic aspects of Angelman syndrome (AS), its molecula...
"Angelman syndrome" (AS) is a neurodevelopmental disorder whose main features are intellectual disab...
Angelman syndrome is a neurogenetic disorder characterized by developmental delay, severe intellectu...
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