MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome.

Dominguez-Valentin, Mev; Wernhoff, Patrik; Cajal, Andrea R; Kalfayan, Pablo G; Piñero, Tamara A; Gonzalez, Maria L; Ferro, Alejandra; Sammartino, Ines; Causada Calo, Natalia S; Vaccaro, Carlos A

Dominguez-Valentin, Mev; Wernhoff, Patrik; Cajal, Andrea R; Kalfayan, Pablo G; Piñero, Tamara A; Gonzalez, Maria L; Ferro, Alejandra; Sammartino, Ines; Causada Calo, Natalia S; Vaccaro, Carlos A.

Afiliação

Dominguez-Valentin M; Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital , Oslo , Norway.
Wernhoff P; Unit of Muscle Biology, Lund Transgenic Core Facility/Reproductive Immunology, Department of Experimental Medical Science, Lund University , Lund , Sweden.
Cajal AR; Institute of Basic Sciences and Experimental Medicine (ICBME), Instituto Universitario Hospital Italiano , Buenos Aires , Argentina.
Kalfayan PG; Programa de Cancer Hereditario (ProCanHe), Hospital Italiano de Buenos Aires , Buenos Aires , Argentina.
Piñero TA; Programa de Cancer Hereditario (ProCanHe), Hospital Italiano de Buenos Aires , Buenos Aires , Argentina.
Gonzalez ML; Programa de Cancer Hereditario (ProCanHe), Hospital Italiano de Buenos Aires , Buenos Aires , Argentina.
Ferro A; Programa de Cancer Hereditario (ProCanHe), Hospital Italiano de Buenos Aires , Buenos Aires , Argentina.
Sammartino I; Programa de Cancer Hereditario (ProCanHe), Hospital Italiano de Buenos Aires , Buenos Aires , Argentina.
Causada Calo NS; Programa de Cancer Hereditario (ProCanHe), Hospital Italiano de Buenos Aires , Buenos Aires , Argentina.
Vaccaro CA; Programa de Cancer Hereditario (ProCanHe), Hospital Italiano de Buenos Aires , Buenos Aires , Argentina.

Front Oncol ; 6: 189, 2016.

Article em En | MEDLINE | ID: mdl-27606285

Palavras-chave

Ile219Val; Lynch syndrome; MLH1; MSH2; mutation

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE País/Região como assunto: America do sul / Argentina Idioma: En Revista: Front Oncol Ano de publicação: 2016 Tipo de documento: Article

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