Little is known about genetic risk factors for idiopathic normal pressure hydrocephalus (iNPH). We examined whether a copy number loss in intron 2 of the SFMBT1 gene could be a genetic risk for shunt-
Background: Epilepsy in childhood is a common and diverse neurological disorder. We conducted a genetic and phenotype analysis of a Chinese cohort of infants and children with epilepsy. Methods: We co
This experiment is part of the C.elegans behavioural database . For more information and the complete collection of experiments visit http://movement.openworm.org preview link : http
Maintaining taxi homeostasis in neurons is important for maintaining the neuromuscular crosstalk and flight function in Drosophila melanogaster. Transcriptome analysis of taxi show that Adar is one of
This experiment is part of the C.elegans behavioural database. For more information and the complete collection of experiments visit http://movement.openworm.org preview link : https://www.youtub
