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The risk of new‐onset cancer associated with HFE C282Y and H63D mutations: evidence from 87,028 participants

To investigate the association between mutation of HFE (the principal pathogenic gene in hereditary haemochromatosis) and risk of cancer, we conducted a meta‐analysis of all available case–control or cohort studies relating to two missense mutations, C282Y and H63D mutations. Eligible studies were i...

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Detalles Bibliográficos
Publicado en:J Cell Mol Med
Autores principales: Lv, Yang‐Fan, Chang, Xian, Hua, Rui‐Xi, Yan, Guang‐Ning, Meng, Gang, Liao, Xiao‐Yu, Zhang, Xi, Guo, Qiao‐Nan
Formato: Artigo
Lenguaje:Inglês
Publicado: John Wiley and Sons Inc. 2016
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4929296/
https://ncbi.nlm.nih.gov/pubmed/26893171
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.12764
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