Cargando…
Lack of Association between NLGN3, NLGN4, SHANK2 and SHANK3 Gene Variants and Autism Spectrum Disorder in a Chinese Population
Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by deficits in social communication, absence or delay in language development, and stereotyped or repetitive behaviors. Genetic studies show that neurexin-neuroligin (NRXN-NLGN) pathway genes contribute susceptibility to A...
Autores principales: | Liu, Yanyan, Du, Yasong, Liu, Wenwen, Yang, Caohua, Liu, Yan, Wang, Hongyan, Gong, Xiaohong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582503/ https://www.ncbi.nlm.nih.gov/pubmed/23468870 http://dx.doi.org/10.1371/journal.pone.0056639 |
Ejemplares similares
-
Cochlear ribbon synapse maturation requires Nlgn1 and Nlgn3
por: Ramirez, Miguel A., et al.
Publicado: (2022) -
A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort
por: Yu, Jindan, et al.
Publicado: (2011) -
Glioblastoma recurrence correlates with NLGN3 levels
por: Liu, Rui, et al.
Publicado: (2018) -
NLGN3 Upregulates Expression of ADAM10 to Promote the Cleavage of NLGN3 via Activating the LYN Pathway in Human Gliomas
por: Dang, Ning-Ning, et al.
Publicado: (2021) -
Novel human sex-typing strategies based on the autism candidate gene NLGN4X and its male-specific gametologue NLGN4Y
por: Maxeiner, Stephan, et al.
Publicado: (2019)