Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder

BACKGROUND: Autism spectrum disorders (ASDs) are male-biased and genetically heterogeneous. While sequencing of sporadic cases has identified de novo risk variants, the heritable genetic contribution and mechanisms driving the male bias are less understood. Here, we aimed to identify familial and se...

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Detalles Bibliográficos
Autores principales: Werling, Donna M, Lowe, Jennifer K, Luo, Rui, Cantor, Rita M, Geschwind, Daniel H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942516/
https://www.ncbi.nlm.nih.gov/pubmed/24533643
http://dx.doi.org/10.1186/2040-2392-5-13

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3942516/
https://www.ncbi.nlm.nih.gov/pubmed/24533643
http://dx.doi.org/10.1186/2040-2392-5-13

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