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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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| Publicado no: | J Cell Mol Med |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2016
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| Assuntos: | |
| Acesso em linha: | 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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