Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia

Schizophrenia (SCZ) is a severe, highly heritable psychiatric disorder. Elucidation of the genetic architecture of the disorder will facilitate greater understanding of the altered underlying neurobiological mechanisms. The aim of this study was to identify likely aetiological variants in subjects a...

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Detalles Bibliográficos
Autores principales: Al Eissa, Mariam M., Fiorentino, Alessia, Sharp, Sally I., O'Brien, Niamh L., Wolfe, Kate, Giaroli, Giovanni, Curtis, David, Bass, Nicholas J., McQuillin, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5813151/
https://www.ncbi.nlm.nih.gov/pubmed/29148569
http://dx.doi.org/10.1111/ahg.12226

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5813151/
https://www.ncbi.nlm.nih.gov/pubmed/29148569
http://dx.doi.org/10.1111/ahg.12226

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