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Development of a multiplex ARMS test for mutations in the HFE gene associated with hereditary haemochromatosis.
Genetic testing for hereditary haemochromatosis is likely to be a significant workload for diagnostic laboratories. The C282Y and H63D mutations in the HFE gene associated with hereditary haemochromatosis have previously been detected using a number of methods including alterations in the restrictio...
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| Publicado no: | J Clin Pathol |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
1998
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC500436/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9577377/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jcp.51.1.73 |
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