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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2012
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| Materias: | |
| 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 |