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A191 NEXT GENERATION SEQUENCING IN THE INVESTIGATION OF HYPERFERRITINEMIA
BACKGROUND: Hyperferritinemia is common and often suggests the diagnosis of iron overload. However, many times it is elevated secondary to inflammation, obesity, alcohol use, or unknown causes. Most Caucasian patients with iron overload are homozygotes for the C282Y mutation of the HFE gene. There a...
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| Vydáno v: | J Can Assoc Gastroenterol |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6508043/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jcag/gwy008.192 |
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