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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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| izdano v: | Frontline Gastroenterol |
|---|---|
| Main Authors: | , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BMJ Publishing Group
2018
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| Teme: | |
| Online dostop: | 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 |
| Oznake: |
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