Study of Bil-Uridine Diphosphate Glucuronyl Transferase (BILUDGPT- 1) Mutation in Neonatal Hyperbilirubinaemia with Glucose-6-Phosphate Dehydrogenase Deficiency.
Gilbert syndrome is caused by defects in the uridine diphosphate- glucuronosyltransferase 1A1 (UGT1A1) gene. These mutations differ among different populations and many of them have been found to be genetic risk factors for the development of neonatal jaundice.
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| Format: | Monograph |
| Language: | en |
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Universiti Sains Malaysia
2005
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| Online Access: | http://eprints.usm.my/10885/1/Study%20of%20Bil-Uridine%20Diphosphate%20Glucuronyl%20Transferase.pdf http://eprints.usm.my/10885/ |
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| _version_ | 1834437357475987456 |
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| author | Mohd Yusoff, Dr Narazah |
| author_facet | Mohd Yusoff, Dr Narazah |
| author_sort | Mohd Yusoff, Dr Narazah |
| building | Hamzah Sendut Library |
| collection | Institutional Repository |
| content_provider | Universiti Sains Malaysia |
| content_source | USM Institutional Repository |
| continent | Asia |
| country | Malaysia |
| description | Gilbert syndrome is caused by defects in the uridine diphosphate- glucuronosyltransferase 1A1 (UGT1A1) gene. These mutations differ among different populations and many of them have been found to be genetic risk factors for the development of neonatal jaundice. |
| format | Monograph |
| id | my.usm.eprints.10885 |
| institution | Universiti Sains Malaysia |
| language | en |
| publishDate | 2005 |
| publisher | Universiti Sains Malaysia |
| record_format | eprints |
| spelling | my.usm.eprints.10885 http://eprints.usm.my/10885/ Study of Bil-Uridine Diphosphate Glucuronyl Transferase (BILUDGPT- 1) Mutation in Neonatal Hyperbilirubinaemia with Glucose-6-Phosphate Dehydrogenase Deficiency. Mohd Yusoff, Dr Narazah R735-854 Medical education. Medical schools. Research Gilbert syndrome is caused by defects in the uridine diphosphate- glucuronosyltransferase 1A1 (UGT1A1) gene. These mutations differ among different populations and many of them have been found to be genetic risk factors for the development of neonatal jaundice. Universiti Sains Malaysia 2005 Monograph NonPeerReviewed application/pdf en http://eprints.usm.my/10885/1/Study%20of%20Bil-Uridine%20Diphosphate%20Glucuronyl%20Transferase.pdf Mohd Yusoff, Dr Narazah (2005) Study of Bil-Uridine Diphosphate Glucuronyl Transferase (BILUDGPT- 1) Mutation in Neonatal Hyperbilirubinaemia with Glucose-6-Phosphate Dehydrogenase Deficiency. Project Report. Universiti Sains Malaysia. |
| spellingShingle | R735-854 Medical education. Medical schools. Research Mohd Yusoff, Dr Narazah Study of Bil-Uridine Diphosphate Glucuronyl Transferase (BILUDGPT- 1) Mutation in Neonatal Hyperbilirubinaemia with Glucose-6-Phosphate Dehydrogenase Deficiency. |
| title | Study of Bil-Uridine Diphosphate Glucuronyl Transferase (BILUDGPT- 1) Mutation in Neonatal Hyperbilirubinaemia with Glucose-6-Phosphate Dehydrogenase Deficiency. |
| title_full | Study of Bil-Uridine Diphosphate Glucuronyl Transferase (BILUDGPT- 1) Mutation in Neonatal Hyperbilirubinaemia with Glucose-6-Phosphate Dehydrogenase Deficiency. |
| title_fullStr | Study of Bil-Uridine Diphosphate Glucuronyl Transferase (BILUDGPT- 1) Mutation in Neonatal Hyperbilirubinaemia with Glucose-6-Phosphate Dehydrogenase Deficiency. |
| title_full_unstemmed | Study of Bil-Uridine Diphosphate Glucuronyl Transferase (BILUDGPT- 1) Mutation in Neonatal Hyperbilirubinaemia with Glucose-6-Phosphate Dehydrogenase Deficiency. |
| title_short | Study of Bil-Uridine Diphosphate Glucuronyl Transferase (BILUDGPT- 1) Mutation in Neonatal Hyperbilirubinaemia with Glucose-6-Phosphate Dehydrogenase Deficiency. |
| title_sort | study of bil-uridine diphosphate glucuronyl transferase (biludgpt- 1) mutation in neonatal hyperbilirubinaemia with glucose-6-phosphate dehydrogenase deficiency. |
| topic | R735-854 Medical education. Medical schools. Research |
| url | http://eprints.usm.my/10885/1/Study%20of%20Bil-Uridine%20Diphosphate%20Glucuronyl%20Transferase.pdf http://eprints.usm.my/10885/ |
| url_provider | http://eprints.usm.my/ |