Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism
Recurrent copy number variations (CNVs) of human 16p11.2 have been associated with a variety of developmental/neurocognitive syndromes. In particular, deletion of 16p11.2 is found in patients with autism, developmental delay, and obesity. Patients with deletions or duplications have a wide range of...
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| Auteurs principaux: | , , , , , , , , , , |
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| Format: | Artigo |
| Langue: | anglais |
| Publié: |
2011
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| Accès en ligne: | https://doi.org/10.1073/pnas.1114042108 |
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