Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism

Autism spectrum disorder (ASD) is a highly heritable neurodevelopmental disorder. Large genetically informative cohorts of individuals with ASD have led to the identification of a limited number of common genome-wide significant (GWS) risk loci to date. However, many more common genetic variants are...

Descripción completa

Detalles Bibliográficos
Autores principales: Matoba, Nana, Liang, Dan, Sun, Huaigu, Aygün, Nil, McAfee, Jessica C., Davis, Jessica E., Raffield, Laura M., Qian, Huijun, Piven, Joseph, Li, Yun, Kosuri, Sriam, Won, Hyejung, Stein, Jason L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400671/
https://www.ncbi.nlm.nih.gov/pubmed/32747698
http://dx.doi.org/10.1038/s41398-020-00953-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7400671/
https://www.ncbi.nlm.nih.gov/pubmed/32747698
http://dx.doi.org/10.1038/s41398-020-00953-9

Ejemplares similares