Cargando…
An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males
BACKGROUND: Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder with a strong genetic component. The skewed prevalence toward males and evidence suggestive of linkage to the X chromosome in some studies suggest the presence of X-linked susceptibility genes in people with ASD. MET...
Autores principales: | Chung, Ren-Hua, Ma, Deqiong, Wang, Kai, Hedges, Dale J, Jaworski, James M, Gilbert, John R, Cuccaro, Michael L, Wright, Harry H, Abramson, Ruth K, Konidari, Ioanna, Whitehead, Patrice L, Schellenberg, Gerard D, Hakonarson, Hakon, Haines, Jonathan L, Pericak-Vance, Margaret A, Martin, Eden R |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3305893/ https://www.ncbi.nlm.nih.gov/pubmed/22050706 http://dx.doi.org/10.1186/2040-2392-2-18 |
Ejemplares similares
-
A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism
por: Hussman, John P, et al.
Publicado: (2011) -
Copy Number Variants in Extended Autism Spectrum Disorder Families Reveal Candidates Potentially Involved in Autism Risk
por: Salyakina, Daria, et al.
Publicado: (2011) -
Investigation of autism and GABA receptor subunit genes in multiple ethnic groups
por: Collins, Ann L., et al.
Publicado: (2006) -
Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants
por: Griswold, Anthony J., et al.
Publicado: (2015) -
Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci
por: Hedges, Dale J, et al.
Publicado: (2012)