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Fatty liver in H63D homozygotes with hyperferritinemia
To study the clinical correlates of the H63D mu-tation we have analysed the phenotype of H63D homo-zygotes identified through mutation analysis in a referral laboratory. A total of 366 blood samples referred for HFE analysis were screened for C282Y and H63D mutations. Four H63D homozygotes were iden...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Co., Limited
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4124361/ https://ncbi.nlm.nih.gov/pubmed/16586555 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v12.i11.1788 |
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