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Neuropathology of 16p13.11 Deletion in Epilepsy
16p13.11 genomic copy number variants are implicated in several neuropsychiatric disorders, such as schizophrenia, autism, mental retardation, ADHD and epilepsy. The mechanisms leading to the diverse clinical manifestations of deletions and duplications at this locus are unknown. Most studies favour...
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| Autores principales: | , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Public Library of Science
2012
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3327721/ https://ncbi.nlm.nih.gov/pubmed/22523559 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0034813 |
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