Absence of the CHEK2 c.1100delC mutation in familial breast and ovarian cancer in Colombia: a case-control study
Background: BRCA1 and BRCA2 have been identified as high-penetrance breast cancer predisposition genes, but they only account for a small fraction of the inherited component of breast cancer. To explain the remaining cases, a polygenic model with a large number of low-to moderate-penetrance genes ha...
- Autores:
-
Rivera Herrera, Ana Lucia
Cifuentes Cardona, Laura Fernanda
Gil Vera, J. A.
Barreto, Guillermo
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2023
- Institución:
- Universidad Cooperativa de Colombia
- Repositorio:
- Repositorio UCC
- Idioma:
- OAI Identifier:
- oai:repository.ucc.edu.co:20.500.12494/50416
- Acceso en línea:
- https://doi.org/10.12688/f1000research.13368.1
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85062855251&doi=10.12688%2ff1000research.13368.1&partnerID=40&md5=8f6e11e47f8c350bfe93dda0ec915e52
https://hdl.handle.net/20.500.12494/50416
- Palabra clave:
- ADULT
AGE
ALLELE SPECIFIC POLYMERASE CHAIN REACTION
ARTICLE
BREAST CANCER
CANCER RISK
CANCER SCREENING
CANCER SUSCEPTIBILITY
CLINICAL FEATURE
COHORT ANALYSIS
COLOMBIA
CONTROLLED STUDY
CROSS-SECTIONAL STUDY
CHECKPOINT KINASE 2
CHEK2 GENE
FEMALE
GENE FUNCTION
GENE MUTATION
GENETIC SCREENING
GENOTYPE
HETEROZYGOTE
HOMOZYGOTE
HUMAN
MAJOR CLINICAL STUDY
OVARY CANCER
RISK FACTOR
SEX
SOCIAL STATUS
- Rights
- openAccess
- License
- http://purl.org/coar/access_right/c_abf2