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.
| Main Author: | |
|---|---|
| Format: | Monograph |
| Language: | English |
| Published: |
Universiti Sains Malaysia
2005
|
| Subjects: | |
| Online Access: | http://eprints.usm.my/10885/1/Study%20of%20Bil-Uridine%20Diphosphate%20Glucuronyl%20Transferase.pdf |
| _version_ | 1825828784370089984 |
|---|---|
| author | Mohd Yusoff, Dr Narazah |
| author_facet | Mohd Yusoff, Dr Narazah |
| author_sort | Mohd Yusoff, Dr Narazah |
| collection | USM |
| 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. |
| first_indexed | 2024-03-06T13:58:45Z |
| format | Monograph |
| id | usm.eprints-10885 |
| institution | Universiti Sains Malaysia |
| language | English |
| last_indexed | 2024-03-06T13:58:45Z |
| publishDate | 2005 |
| publisher | Universiti Sains Malaysia |
| record_format | dspace |
| spelling | usm.eprints-108852019-05-08T03:23:39Z 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 |
| work_keys_str_mv | AT mohdyusoffdrnarazah studyofbiluridinediphosphateglucuronyltransferasebiludgpt1mutationinneonatalhyperbilirubinaemiawithglucose6phosphatedehydrogenasedeficiency |