CRIGLER- NAJJAR SYNDROME - CASE REPORT
Crigler-Najjar syndrome is a rare genetic disorder that causes severe unconjugated hyperbilirubinaemia. The syndrome is caused by a mutation in the UGT1A1 gene, which results in a deficiency or complete lack of the UGT1A1 enzyme, which is responsible for the conjugation of bilirubin. If the disease...
-д хадгалсан:
| Үндсэн зохиолчид: | , |
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| Формат: | Ном |
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The Society for Children with Metabolic Disorders,
2022-05-01T00:00:00Z.
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| Онлайн хандалт: | Connect to this object online. |
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Шошго нэмэх
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Интернэт
Connect to this object online.3rd Floor Main Library
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A1234.567 |
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| Хуулбар 1 | Бэлэн |