Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome.
The aim of this work was to evaluate the influence of abnormal UDP-glucoronosyltransferase-1 (UGT1A1) gene variant, on the incidence and severity of neonatal hyperbilirubinemia, in glucose-6-phosphate dehydrogenase (G6PD) deficient newborns. The A(TA)nTAA region in the promoter of the UGT1A1 gene wa...
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| Outros Autores: | , , , , , , |
| Formato: | article |
| Idioma: | por |
| Publicado em: |
2002
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| Texto completo: | https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/1986 |
| País: | Portugal |
| Oai: | oai:ojs.www.actamedicaportuguesa.com:article/1986 |