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J-GLOBAL ID:201702291075450525   Reference number:17A0139194

自閉スペクトラム症多発罹患家系の全エクソームシークエンスおよびフォローアップ研究

Author (13):
Material:
Volume: 119  Issue:Page: 3-8  Publication year: Jan. 25, 2017 
JST Material Number: Z0692A  ISSN: 0033-2658  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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JST classification (3):
JST classification
Category name(code) classified by JST.
Mental disorders  ,  Congenital diseases,deformities in general.  ,  Genetic variation 
Reference (24):
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  • Choesmel, V., Fribourg, S., Aguissa-Toure, A. H., et al. : Mutation of ribosomal protein RPS24 in Diamond-Blackfan anemia results in a ribosome biogenesis disorder. Hum Mol Genet, 17 ; 1253-1263, 2008
  • Cirulli, E. T., Goldstein, D. B. : Uncovering the roles of rare variants in common disease through wholegenome sequencing. Nat Rev Genet, 11 ; 415-425, 2010
  • Cruchaga, C., Karch, C. M., Jin, S. C., et al. : Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease. Nature, 505 ; 550-554, 2014
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