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Mutations in the TSGA14 gene in families with autism spectrum disorders
Linkage to 7q has been the most robust genetic finding in familial autism. A previous scan of multiplex families with autism spectrum disorders found a linkage signal of genome-wide significance at D7S530 on 7q32. We searched a candidate imprinted region at this location for genetic variants in fami...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3552624/ https://ncbi.nlm.nih.gov/pubmed/21438139 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.31162 |
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