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The clinical management of hereditary haemochromatosis
Hereditary haemochromatosis is an autosomal recessive disorder with variable penetrance. Most patients are C282Y homozygotes while heterozygotes or patients who are homozygous with other mutations are uncommonly affected. The true genotype to phenotype expression remains unclear. Treatment with phle...
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| Gepubliceerd in: | Frontline Gastroenterol |
|---|---|
| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BMJ Publishing Group
2018
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5868443/ https://ncbi.nlm.nih.gov/pubmed/29588838 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/flgastro-2017-100872 |
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