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Alu element insertion in the MLH1 exon 6 coding sequence as a mutation predisposing to Lynch syndrome.
Solassol, Jérôme; Larrieux, Marion; Leclerc, Julie; Ducros, Vincent; Corsini, Carole; Chiésa, Jean; Pujol, Pascal; Rey, Jean-Marc.
Afiliación
  • Solassol J; Department of Pathology and Oncobiology, Montpellier University Hospital, Montpellier, France.
  • Larrieux M; IRCM Inserm, Montpellier University, Montpellier, France.
  • Leclerc J; Department of Pathology and Oncobiology, Montpellier University Hospital, Montpellier, France.
  • Ducros V; Department of Biochemistry and Molecular Biology, and Inserm UMR-S, Lille University Hospital, JPA Research Center, Lille University, Lille, France.
  • Corsini C; Department of Pathology and Oncobiology, Montpellier University Hospital, Montpellier, France.
  • Chiésa J; Department of Genetics, Montpellier University Hospital, Montpellier, France.
  • Pujol P; Department of Cytogenetics, Nimes University Hospital, Nîmes, France.
  • Rey JM; Department of Genetics, Montpellier University Hospital, Montpellier, France.
Hum Mutat ; 40(6): 716-720, 2019 06.
Article en En | MEDLINE | ID: mdl-30815977
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales Hereditarias sin Poliposis / Mutagénesis Insercional / Análisis de Secuencia de ADN / Homólogo 1 de la Proteína MutL Tipo de estudio: Prognostic_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Francia
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales Hereditarias sin Poliposis / Mutagénesis Insercional / Análisis de Secuencia de ADN / Homólogo 1 de la Proteína MutL Tipo de estudio: Prognostic_studies Límite: Adult / Female / Humans / Male Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Francia