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Open Access
Peer-reviewed
Research Article
Mexican BRCA1 founder mutation: Shortening the gap in genetic assessment for hereditary breast and ovarian cancer patients
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Veronica Fragoso-Ontiveros ,
Contributed equally to this work with: Veronica Fragoso-Ontiveros, Jose Antonio Velázquez-Aragón
Roles Conceptualization, Formal analysis, Investigation, Methodology, Supervision, Writing – review & editing
Affiliation Hereditary Cancer Clinic, National Cancer Institute, Mexico city, Mexico
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Jose Antonio Velázquez-Aragón ,
Contributed equally to this work with: Veronica Fragoso-Ontiveros, Jose Antonio Velázquez-Aragón
Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Validation, Writing – review & editing
Affiliation Molecular Biology Laboratory, National Paediatrics Institute, Mexico city, Mexico
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Paulina Maria Nuñez-Martínez,
Roles Investigation, Methodology, Validation, Writing – review & editing
Affiliation Hereditary Cancer Clinic, National Cancer Institute, Mexico city, Mexico
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Maria de la Luz Mejía-Aguayo,
Roles Investigation, Methodology, Writing – review & editing
Affiliation Hereditary Cancer Clinic, National Cancer Institute, Mexico city, Mexico
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Silvia Vidal-Millán,
Roles Investigation, Methodology, Writing – review & editing
Affiliation Hereditary Cancer Clinic, National Cancer Institute, Mexico city, Mexico
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Abraham Pedroza-Torres,
Roles Data curation, Investigation, Methodology, Writing – review & editing
Affiliation Research Direction, National Cancer Institute, Mexico city, Mexico
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Yuliana Sánchez-Contreras,
Roles Investigation, Project administration, Writing – review & editing
Affiliation Hereditary Cancer Clinic, National Cancer Institute, Mexico city, Mexico
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Miguel Angel Ramírez-Otero,
Roles Data curation, Formal analysis, Writing – review & editing
Affiliation Hereditary Cancer Clinic, National Cancer Institute, Mexico city, Mexico
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Rodolfo Muñiz-Mendoza,
Roles Investigation, Writing – review & editing
Affiliation Research Direction, National Cancer Institute, Mexico city, Mexico
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Julieta Domínguez-Ortíz,
Roles Investigation, Writing – review & editing
Affiliation Hereditary Cancer Clinic, National Cancer Institute, Mexico city, Mexico
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Talia Wegman-Ostrosky,
Roles Investigation, Writing – review & editing
Affiliation Hereditary Cancer Clinic, National Cancer Institute, Mexico city, Mexico
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Juan Enrique Bargalló-Rocha,
Roles Investigation, Writing – review & editing
Affiliation Breast Cancer Department, National Cancer Institute, Mexico city, Mexico
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Dolores Gallardo-Rincón,
Roles Investigation, Writing – review & editing
Affiliation Medical Oncology Department, National Cancer Institute, Mexico city, Mexico
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Nancy Reynoso-Noveron,
Roles Formal analysis, Investigation, Methodology, Writing – review & editing
Affiliation Epidemiology Department, National Cancer Institute, Mexico city, Mexico
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Cristian Arriaga-Canon,
Roles Investigation, Writing – review & editing
Affiliation Research Direction, National Cancer Institute, Mexico city, Mexico
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Abelardo Meneses-García,
Roles Investigation, Writing – review & editing
Affiliation General Direction, National Cancer Institute, Mexico city, Mexico
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Luis Alonso Herrera-Montalvo,
Roles Investigation, Writing – review & editing
Affiliation Research Direction, National Cancer Institute, Mexico city, Mexico
⨯ - [ ... ],
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Rosa Maria Alvarez-Gomez
Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing
* E-mail: rosamag2@hotmail.com
Affiliation Hereditary Cancer Clinic, National Cancer Institute, Mexico city, Mexico
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Mexican BRCA1 founder mutation: Shortening the gap in genetic assessment for hereditary breast and ovarian cancer patients
- Veronica Fragoso-Ontiveros,
- Jose Antonio Velázquez-Aragón,
- Paulina Maria Nuñez-Martínez,
- Maria de la Luz Mejía-Aguayo,
- Silvia Vidal-Millán,
- Abraham Pedroza-Torres,
- Yuliana Sánchez-Contreras,
- Miguel Angel Ramírez-Otero,
- Rodolfo Muñiz-Mendoza,
- Julieta Domínguez-Ortíz
- Published: September 23, 2019
- https://doi.org/10.1371/journal.pone.0222709