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Primary haemochromatosis - causes, symptoms, diagnosis, treatment

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Mgr inż. Edyta Żyromska

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Primary haemochromatosis - causes, symptoms, diagnosis, treatment

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Erythrocytes

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Gen c282y Hfe gene Metabolic diseases Mutation Primary haemochromatosis
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REFERENCES

Casu C. et al.: Hepcidin agonists as therapeutic tools, 'Blood' 2018; doi: 10.1182/blood-2017-11-737411.

Sources

https://www.su.krakow.pl/system/files/14925/0d88cf1402.pdf?1446202568

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