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Drosophila Homolog of Human KIF22 at the Autism-Linked 16p11.2 Loci Influences Synaptic Connectivity at Larval Neuromuscular Junctions

Copy number variations at multiple chromosomal loci, including 16p11.2, have recently been implicated in the pathogenesis of autism spectrum disorder (ASD), a neurodevelopmental disease that affects 1~3% of children worldwide. The aim of this study was to investigate the roles of human genes at the...

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Detalles Bibliográficos
Autores principales: Park, Sang Mee, Littleton, J. Troy, Park, Hae Ryoun, Lee, Ji Hye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Brain and Neural Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766112/
https://www.ncbi.nlm.nih.gov/pubmed/26924931
http://dx.doi.org/10.5607/en.2016.25.1.33