Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder

BACKGROUND: Autism spectrum disorder (ASD) is highly heritable, but the genetic risk factors for it remain largely unknown. Although structural variants with large effect sizes may explain up to 15% ASD, genome-wide association studies have failed to uncover common single nucleotide variants with la...

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Detalles Bibliográficos
Autores principales: Steinberg, Karyn Meltz, Ramachandran, Dhanya, Patel, Viren C, Shetty, Amol C, Cutler, David J, Zwick, Michael E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492087/
https://www.ncbi.nlm.nih.gov/pubmed/23020841
http://dx.doi.org/10.1186/2040-2392-3-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492087/
https://www.ncbi.nlm.nih.gov/pubmed/23020841
http://dx.doi.org/10.1186/2040-2392-3-8

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