Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders

Both schizophrenia (SCZ) and autism spectrum disorders (ASD) are neuropsychiatric disorders with overlapping genetic etiology. Protocadherin 15 (PCDH15), which encodes a member of the cadherin super family that contributes to neural development and function, has been cited as a risk gene for neurops...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:PLoS One
Κύριοι συγγραφείς: Ishizuka, Kanako, Kimura, Hiroki, Wang, Chenyao, Xing, Jingrui, Kushima, Itaru, Arioka, Yuko, Oya-Ito, Tomoko, Uno, Yota, Okada, Takashi, Mori, Daisuke, Aleksic, Branko, Ozaki, Norio
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Public Library of Science 2016
Θέματα:
Research Article
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4825995/
https://ncbi.nlm.nih.gov/pubmed/27058588
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0153224
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