A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE Hereditary Haemochromatosis

There is emerging evidence that there are genetic modifiers of iron indices for HFE gene mutation carriers at risk of hereditary hemochromatosis. A random sample stratified by HFE genotype of 863 from a cohort of 31,192 people of northern European descent provided blood samples for genotyping of 476...

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Main Authors: Constantine, C. C., Anderson, G. J., Vulpe, C. D., McLaren, C. E., Bahlo, M., Yeap, H. L., Gertig, D. M., Osborne, N. J., Bertalli, N. A., Beckman, K. B., Chen, V., Matak, P., McKie, A. T., Delatycki, M. B., Olynyk, J. K., English, D. R., Southey, M. C., Giles, G. G., Hopper, J. L., Allen, K. J., Gurrin, L. C.
Formato: Artigo
Idioma:English
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2767327/
https://ncbi.nlm.nih.gov/pubmed/19673882
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2141.2009.07843.x
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https://ncbi.nlm.nih.gov/pmc/articles/PMC2767327/
https://ncbi.nlm.nih.gov/pubmed/19673882
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2141.2009.07843.x

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