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Familial screening for genetic haemochromatosis by means of DNA markers.
Genetic haemochromatosis (HFE) is a frequent and potentially fatal disease. Early phlebotomies may prevent complications. The recessive gene for HFE is unknown but closely linked to the HLA-A locus. No direct test for homozygosity for HFE is currently available, apart from HLA typing within the fami...
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| Pubblicato in: | J Med Genet |
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| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BMJ Publishing Group
1992
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1015951/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1349923/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.29.5.320 |
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