A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome
| Image |  |
|---|---|
| Description | scientific article published on 20 July 2011 |
| Author/s |
author: Ichiro Morioka |
| Publication date | July 20, 2011 |
| Language | |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |