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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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Detalles Bibliográficos
Autores principales:	Liu, Joan Y. W., Kasperavičiūtė, Dalia, Martinian, Lillian, Thom, Maria, Sisodiya, Sanjay M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2012
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3327721/ https://www.ncbi.nlm.nih.gov/pubmed/22523559 http://dx.doi.org/10.1371/journal.pone.0034813

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