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Contribution of G71R mutation to Gilbert’s syndrome phenotype in a Greek patient: A case report
Gilbert’s syndrome is characterized by a benign indirect hyperbilirubinemia. It has often been underestimated and undiagnosed because of its mild symptoms; although it is not as rare as was once believed when its frequency was estimated using data originating from biochemical tests. Based on molecul...
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| Autori principali: | , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Baishideng Publishing Group Co., Limited
2011
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3205121/ https://ncbi.nlm.nih.gov/pubmed/22046580 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4292/wjgpt.v2.i5.42 |
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