Detection of the jaundice-related G71R mutation in the UGT1A1 gene by denaturing high performance liquid chromatography (DHPLC)
Background The G71R mutation in the UGT1A1 gene has been associated with neonatal jaundice and other cases of hereditary, unconjugated hyperbilirubinemia in several Asian populations. Currently, DNA sequencing is the only method available to identify the mutation, which can be time-...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Indonesian Pediatric Society Publishing House,
2009-03-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |