A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci

BACKGROUND: Breast cancer is the most common cancer in women worldwide. Around 50% of breast cancer familial risk has been so far explained by known susceptibility alleles with variable levels of risk and prevalence. The vast majority of these breast cancer associated variations reported to date are...

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Detalles Bibliográficos
Autores principales: Hamdi, Yosr, Ben Rekaya, Mariem, Jingxuan, Shan, Nagara, Majdi, Messaoud, Olfa, Benammar Elgaaied, Amel, Mrad, Ridha, Chouchane, Lotfi, Boubaker, Mohamed Samir, Abdelhak, Sonia, Boussen, Hamouda, Romdhane, Lilia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310952/
https://www.ncbi.nlm.nih.gov/pubmed/30594178
http://dx.doi.org/10.1186/s12885-018-5133-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6310952/
https://www.ncbi.nlm.nih.gov/pubmed/30594178
http://dx.doi.org/10.1186/s12885-018-5133-8

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