FOXG1 Syndrome (FS) is a devastating neurodevelopmental disorder that is caused by a heterozygous loss-of-function (LOF) mutation of the FOXG1 pet calming peanut butter gene, which encodes a transcriptional regulator important for telencephalic brain development.People with FS have marked developmental delays, impaired ambulation, movement disorder
Infantile spasms are characterized by age-specific expression of epileptic spasms and hypsarrhythmia and often result in significant cognitive impairment.Other epilepsies or autism often ensue especially in symptomatic IS (SIS).Cortical or subcortical damage, including white matter, have been implicated in the pathogenesis of SIS.To generate a mode
Serological assays detecting neutralising antibodies are important for determining the immune responses following infection or vaccination and are also often considered a correlate of protection.The target of neutralising antibodies is usually located in the Envelope protein on the viral surface, which mediates cell entry.As such, presentation of t