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Screening for genetic haemochromatosis in blood samples with raised alanine aminotransferase
BACKGROUND—In the UK approximately 1 in 140 people are homozygous for the C282Y mutation of the HFE gene and are at risk from iron overload caused by genetic haemochromatosis (GH). Early detection can prevent organ damage secondary to iron deposition and increase life expectancy. AIM—To screen for G...
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| Autori principali: | , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2000
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1727938/ https://ncbi.nlm.nih.gov/pubmed/10764716 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/gut.46.5.707 |
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