Investigation of single-nucleotide variants in MBD5 associated with autism spectrum disorders and schizophrenia phenotypes.

Ishizuka, Kanako; Kimura, Hiroki; Yoshimi, Akira; Banno, Masahiro; Kushima, Itaru; Uno, Yota; Okada, Takashi; Mori, Daisuke; Aleksic, Branko; Ozaki, Norio

Ishizuka, Kanako; Kimura, Hiroki; Yoshimi, Akira; Banno, Masahiro; Kushima, Itaru; Uno, Yota; Okada, Takashi; Mori, Daisuke; Aleksic, Branko; Ozaki, Norio.

Afiliação

Ishizuka K; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kimura H; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yoshimi A; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Banno M; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kushima I; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Uno Y; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Okada T; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Mori D; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Aleksic B; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Ozaki N; Department of Psychiatry, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Nagoya J Med Sci ; 78(4): 465-474, 2016 Dec.

Article em En | MEDLINE | ID: mdl-28008202

Palavras-chave

genotype-phenotype correlations; neurodevelopmental disorders; next-generation sequencing technology; rare variants

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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Nagoya J Med Sci Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Japão

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