RE: frameshift variant FANCL*c.1096_1099dupATTA is not associated with high breast cancer risk.

Zemankova, P; Lhota, F; Kleiblova, P; Soukupova, J; Vocka, M; Janatova, M; Kleibl, Z

Zemankova, P; Lhota, F; Kleiblova, P; Soukupova, J; Vocka, M; Janatova, M; Kleibl, Z.

Afiliação

Zemankova P; Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.
Lhota F; Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.
Kleiblova P; Centre for Medical Genetics and Reproductive Medicine GENNET, Prague, Czech Republic.
Soukupova J; Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.
Vocka M; Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.
Janatova M; Institute of Biochemistry and Experimental Oncology, First Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.
Kleibl Z; Department of Oncology, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Prague, Czech Republic.

Clin Genet ; 90(4): 387-9, 2016 10.

Article em En | MEDLINE | ID: mdl-27659787

Assuntos

Proteína do Grupo de Complementação L da Anemia de Fanconi/genética; Anemia de Fanconi; Neoplasias da Mama; Mutação da Fase de Leitura; Humanos

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína do Grupo de Complementação L da Anemia de Fanconi / Anemia de Fanconi Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Clin Genet Ano de publicação: 2016 Tipo de documento: Article País de afiliação: República Tcheca

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