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Combined effect of regulatory polymorphisms on transcription of <it>UGT1A1 </it>as a cause of Gilbert syndrome
<p>Abstract</p> <p>Background</p> <p>Gilbert syndrome is caused by defects in bilirubin UDP-glucuronosyltransferase (UGT1A1). The most common variation believed to be involved is A(TA)7TAA. Although several polymorphisms have been found to link with A(TA)7TAA, the combi...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMC
2010-06-01
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| Colecção: | BMC Gastroenterology |
| Acesso em linha: | http://www.biomedcentral.com/1471-230X/10/57 |
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