Art
J-GLOBAL ID:201702226882043302   Reference number:17A1408606

Deep sequencing reveals variations in somatic cell mosaic mutations between monozygotic twins with discordant psychiatric disease

ディープシークエンシングは精神医学的疾患が一致しない一卵性双生児間の体細胞モザイク変異の変化を明らかにする
Author (12):
Material:
Volume:Issue: July  Page: WEB ONLY  Publication year: Jul. 2017 
JST Material Number: U1014A  ISSN: 2054-345X  Document type: Article
Article type: 原著論文  Country of issue: Germany, Federal Republic of (DEU)  Language: ENGLISH (EN)
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JST classification (2):
JST classification
Category name(code) classified by JST.
Genetic variation  ,  Mental disorders 
Reference (38):
  • Shih RA, Belmonte PL, Zandi PP. A review of the evidence from family, twin and adoption studies for a genetic contribution to adult psychiatric disorders. Int Rev Psychiatry 2004; 16: 260-283.
  • Steffenburg S, Gillberg C, Hellgren L, Andersson L, Gillberg IC, Jakobsson G et al. A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. J Child Psychol Psychiatry 1989; 30: 405-416.
  • Bailey A, Le Couteur A, Gottesman I, Bolton P, Simonoff E, Yuzda E et al. Autism as a strongly genetic disorder: evidence from a British twin study. Psychol Med 1995; 25: 63-77.
  • Coolidge FL, Thede LL, Young SE. The heritability of gender identity disorder in a child and adolescent twin sample. Behav Genet 2002; 32: 251-257.
  • Kondo S, Schutte BC, Richardson RJ, Bjork, Knight AS, Watanabe Y et al. Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nat Genet 2002; 32: 285-289.
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