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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Библиографические подробности
Опубликовано в: :BMC Cancer
Главные авторы: 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
Формат: Artigo
Язык:Inglês
Опубликовано: BioMed Central 2018
Предметы:
Research Article
Online-ссылка: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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