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Rare inherited variation in autism: beginning to see the forest and a few trees
In this issue of Neuron, two papers (Lim et al. 2013, Yu et al. 2013) use whole exome sequencing (WES) to elucidate the contribution of inherited variation to the risk for autism by leveraging the increased penetrance of homozygous and compound heterozygous rare variants in autosomes and hemizygous...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3691080/ https://ncbi.nlm.nih.gov/pubmed/23352155 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuron.2013.01.010 |
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