文献
J-GLOBAL ID:201802213359816283
整理番号:18A1728744
複数の影響を受けた家族,関連研究および機能分析における稀な変異体分析は統合失調症および双極性障害におけるITGβ4遺伝子の役割を示唆する【JST・京大機械翻訳】
Rare variant analysis in multiply affected families, association studies and functional analysis suggest a role for the ITGΒ4 gene in schizophrenia and bipolar disorder
著者 (10件):
O’Brien N.L.
(UCL Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK)
,
Fiorentino A.
(UCL Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK)
,
Curtis D.
(UCL Genetics Institute, University College London, London, UK)
,
Curtis D.
(Centre for Psychiatry, Barts and the London School of Medicine and Dentistry, London, UK)
,
Rayner C.
(UCL Genetics Institute, University College London, London, UK)
,
Petrosellini C.
(UCL Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK)
,
Al Eissa M.
(UCL Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK)
,
Bass N.J.
(UCL Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK)
,
McQuillin A.
(UCL Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK)
,
Sharp S.I.
(UCL Molecular Psychiatry Laboratory, Division of Psychiatry, University College London, London, UK)
資料名:
Schizophrenia Research
(Schizophrenia Research)
巻:
199
ページ:
181-188
発行年:
2018年
JST資料番号:
W3162A
ISSN:
0920-9964
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
オランダ (NLD)
言語:
英語 (EN)