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Haemochromatosis gene mutations in idiopathic dilated cardiomyopathy
BACKGROUND—Two common mutations of the haemochromatosis associated gene (HFE) (cys282tyr (C282Y) and his63asp (H63D)) have been implicated in haemochromatosis and as modulators in cardiovascular disease. OBJECTIVE—To investigate the role of these mutations in the pathogenesis of idiopathic dilated c...
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| Main Authors: | , , , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2000
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1729493/ https://ncbi.nlm.nih.gov/pubmed/11040018 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/heart.84.5.541 |
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