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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Publicado en:BMC Cancer
Main Authors: 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: Artigo
Idioma:Inglês
Publicado: BioMed Central 2018
Assuntos:
Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6310952/
https://ncbi.nlm.nih.gov/pubmed/30594178
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12885-018-5133-8
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