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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Publicat a:Ann Hum Genet
Autors principals: Al Eissa, Mariam M., Fiorentino, Alessia, Sharp, Sally I., O'Brien, Niamh L., Wolfe, Kate, Giaroli, Giovanni, Curtis, David, Bass, Nicholas J., McQuillin, Andrew
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2017
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Original Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5813151/
https://ncbi.nlm.nih.gov/pubmed/29148569
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ahg.12226
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