A carregar...
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...
Na minha lista:
| Main Authors: | , , , , , |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2012
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3492087/ https://ncbi.nlm.nih.gov/pubmed/23020841 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2040-2392-3-8 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|