Cargando…
The CCND1 c.870G risk allele is enriched in individuals of African ancestry with plasma cell dyscrasias
Autores principales: | Baughn, Linda B., Li, Zhuo, Pearce, Kathryn, Vachon, Celine M., Polley, Mei-Yin, Keats, Jonathan, Elhaik, Eran, Baird, Michael, Therneau, Terry, Cerhan, James R., Bergsagel, P. Leif, Dispenzieri, Angela, Rajkumar, S. Vincent, Asmann, Yan W., Kumar, Shaji |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7075993/ https://www.ncbi.nlm.nih.gov/pubmed/32179748 http://dx.doi.org/10.1038/s41408-020-0294-5 |
Ejemplares similares
-
Differences in genomic abnormalities among African individuals with monoclonal gammopathies using calculated ancestry
por: Baughn, Linda B., et al.
Publicado: (2018) -
Polyclonal serum free light chain elevation is associated with increased risk of monoclonal gammopathies
por: Kumar, Shaji, et al.
Publicado: (2019) -
Single Nucleotide Polymorphism (A870G) of the CCND1 gene: association with colorectal cancer susceptibility
por: Montazer Haghighi, Mahdi, et al.
Publicado: (2017) -
The Missing Link of Jewish European Ancestry: Contrasting the Rhineland and
the Khazarian Hypotheses
por: Elhaik, Eran
Publicado: (2013) -
The association between CCND1 G870A polymorphism and colorectal cancer risk: A meta-analysis
por: Xie, Mei, et al.
Publicado: (2017)