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Noncoding Aberrations in Mismatch Repair Genes Underlie a Substantial Part of the Missing Heritability in Lynch Syndrome.
Te Paske, Iris B A W; Mensenkamp, Arjen R; Neveling, Kornelia; Hoogerbrugge, Nicoline; Ligtenberg, Marjolijn J L; De Voer, Richarda M.
Afiliação
  • Te Paske IBAW; Department of Human Genetics, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.
  • Mensenkamp AR; Department of Human Genetics, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.
  • Neveling K; Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition and Behaviour, Nijmegen, the Netherlands.
  • Hoogerbrugge N; Department of Human Genetics, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.
  • Ligtenberg MJL; Department of Human Genetics, Department of Pathology, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.
  • De Voer RM; Department of Human Genetics, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands. Electronic address: Richarda.devoer@radboudumc.nl.
Gastroenterology ; 163(6): 1691-1694.e7, 2022 12.
Article em En | MEDLINE | ID: mdl-36037994
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / Reparo de Erro de Pareamento de DNA Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / Reparo de Erro de Pareamento de DNA Idioma: En Ano de publicação: 2022 Tipo de documento: Article