Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways

Studies of rare genetic variation have identified molecular pathways conferring risk for developmental neuropsychiatric disorders. To date, no published whole-exome sequencing studies have been reported in obsessive-compulsive disorder (OCD). We sequenced all the genome coding regions in 20 sporadic...

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Detalles Bibliográficos
Autores principales: Cappi, C, Brentani, H, Lima, L, Sanders, S J, Zai, G, Diniz, B J, Reis, V N S, Hounie, A G, Conceição do Rosário, M, Mariani, D, Requena, G L, Puga, R, Souza-Duran, F L, Shavitt, R G, Pauls, D L, Miguel, E C, Fernandez, T V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872454/
https://www.ncbi.nlm.nih.gov/pubmed/27023170
http://dx.doi.org/10.1038/tp.2016.30

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4872454/
https://www.ncbi.nlm.nih.gov/pubmed/27023170
http://dx.doi.org/10.1038/tp.2016.30

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