Angelman syndrome (AS) is a neurodevelopmental disorder caused by loss of expression of the maternal copy of the UBE3A gene. Individuals with AS have a multifaceted behavioral phenotype consisting of deficits in motor function, epilepsy, cognitive impairment, sleep abnormalities, as well as other comorbidities. Effectively modeling this behavioral profile and measuring behavioral improvement will be crucial for the success of ongoing and future clinical trials. Foundational studies have defined an array of behavioral phenotypes in the AS mouse model. However, no single behavioral test is able to fully capture the complex nature of AS-in mice, or in children. We performed multidimensional analysis (principal component analysis + k-means clus...
Angelman syndrome (AS) is an inheritable neurodevelopmental disorder resulting from the loss of func...
Angelman syndrome (AS) is an inheritable neurodevelopmental disorder resulting from the loss of func...
Angelman syndrome (AS), a genetic disorder occurring in approximately one in every 15,000 births, is...
Angelman syndrome is a neurodevelopmental disorder presenting with severe deficits in motor, speech,...
Angelman syndrome (AS) is a neurodevelopmental disorder caused by deficits in maternally inherited U...
Angelman syndrome (AS) is a single-gene neurodevelopmental disorder associated with cognitive and mo...
Angelman syndrome (AS) is a single-gene neurodevelopmental disorder associated with cognitive and mo...
Angelman syndrome (AS) is a severe neurodevelopmental disorder associated with disruption of materna...
Abstract Background Angelman syndrome (AS) is a neurodevelopmental disorder caused by mutations affe...
Angelman syndrome (AS) is a severe neurodevelopmental disorder associated with disruption of materna...
Angelman syndrome (AS) is a childhood-onset neurogenetic disorder characterized by functionally seve...
Angelman syndrome (AS) is a childhood-onset neurogenetic disorder characterized by functionally seve...
Angelman syndrome (AS) is a childhood-onset neurogenetic disorder characterized by functionally seve...
Angelman syndrome (AS) is a neurodevelopmental disorder that results from a loss of the paternally i...
Background: Angelman syndrome (AS) is a neurodevelopmental disorder caused by mutations affecting UB...
Angelman syndrome (AS) is an inheritable neurodevelopmental disorder resulting from the loss of func...
Angelman syndrome (AS) is an inheritable neurodevelopmental disorder resulting from the loss of func...
Angelman syndrome (AS), a genetic disorder occurring in approximately one in every 15,000 births, is...
Angelman syndrome is a neurodevelopmental disorder presenting with severe deficits in motor, speech,...
Angelman syndrome (AS) is a neurodevelopmental disorder caused by deficits in maternally inherited U...
Angelman syndrome (AS) is a single-gene neurodevelopmental disorder associated with cognitive and mo...
Angelman syndrome (AS) is a single-gene neurodevelopmental disorder associated with cognitive and mo...
Angelman syndrome (AS) is a severe neurodevelopmental disorder associated with disruption of materna...
Abstract Background Angelman syndrome (AS) is a neurodevelopmental disorder caused by mutations affe...
Angelman syndrome (AS) is a severe neurodevelopmental disorder associated with disruption of materna...
Angelman syndrome (AS) is a childhood-onset neurogenetic disorder characterized by functionally seve...
Angelman syndrome (AS) is a childhood-onset neurogenetic disorder characterized by functionally seve...
Angelman syndrome (AS) is a childhood-onset neurogenetic disorder characterized by functionally seve...
Angelman syndrome (AS) is a neurodevelopmental disorder that results from a loss of the paternally i...
Background: Angelman syndrome (AS) is a neurodevelopmental disorder caused by mutations affecting UB...
Angelman syndrome (AS) is an inheritable neurodevelopmental disorder resulting from the loss of func...
Angelman syndrome (AS) is an inheritable neurodevelopmental disorder resulting from the loss of func...
Angelman syndrome (AS), a genetic disorder occurring in approximately one in every 15,000 births, is...