Population and breast cancer patients’ analysis reveals the diversity of genomic variation of the BRCA genes in the Mexican population

Interpretation of variants of unknown significance (VUS) in genetic tests is complicated in ethnically diverse populations, given the lack of information regarding the common spectrum of genetic variation in clinically relevant genes. Public availability of data obtained from high-throughput genotyp...

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Pubblicato in:Hum Genomics
Autori principali: Fernández-Lopez, J. C., Romero-Córdoba, S., Rebollar-Vega, R., Alfaro-Ruiz, L. A., Jiménez-Morales, S., Beltrán-Anaya, F., Arellano-Llamas, R., Cedro-Tanda, A., Rios-Romero, M., Ramirez-Florencio, M., Bautista-Piña, V., Dominguez-Reyes, C., Villegas-Carlos, F., Tenorio-Torres, A., Hidalgo-Miranda, A.
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2019
Soggetti:
Primary Research
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6327376/
https://ncbi.nlm.nih.gov/pubmed/30630528
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40246-018-0188-9
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