Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility

Background: Nuclear distribution E homolog 1 (NDE1), located within chromosome 16p13.11, plays an essential role in microtubule organization, mitosis, and neuronal migration and has been suggested by several studies of rare copy number variants to be a promising schizophrenia (SCZ) candidate gene. R...

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Detalhes bibliográficos
Publicado no:Schizophr Bull
Main Authors: Kimura, Hiroki, Tsuboi, Daisuke, Wang, Chenyao, Kushima, Itaru, Koide, Takayoshi, Ikeda, Masashi, Iwayama, Yoshimi, Toyota, Tomoko, Yamamoto, Noriko, Kunimoto, Shohko, Nakamura, Yukako, Yoshimi, Akira, Banno, Masahiro, Xing, Jingrui, Takasaki, Yuto, Yoshida, Mami, Aleksic, Branko, Uno, Yota, Okada, Takashi, Iidaka, Tetsuya, Inada, Toshiya, Suzuki, Michio, Ujike, Hiroshi, Kunugi, Hiroshi, Kato, Tadafumi, Yoshikawa, Takeo, Iwata, Nakao, Kaibuchi, Kozo, Ozaki, Norio
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2015
Assuntos:
Regular Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4393687/
https://ncbi.nlm.nih.gov/pubmed/25332407
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/schbul/sbu147
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