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An efficient machine learning-based approach for screening individuals at risk of hereditary haemochromatosis
Hereditary haemochromatosis (HH) is an autosomal recessive disease, where HFE C282Y homozygosity accounts for 80–85% of clinical cases among the Caucasian population. HH is characterised by the accumulation of iron, which, if untreated, can lead to the development of liver cirrhosis and liver cancer...
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| Publicado no: | Sci Rep |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7691515/ https://ncbi.nlm.nih.gov/pubmed/33244054 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-77367-6 |
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