Results
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6441.
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A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome. [electronic resource] by
- Nakagawa, Taku
- Mure, Takeo
- Yusoff, Surini
- Ono, Eiichi
- Kusuma Harahap, Indra Sari
- Morikawa, Satoru
- Morioka, Ichiro
- Takeshima, Yasuhiro
- Nishio, Hisahide
- Matsuo, Masafumi
Producer: 20120404
In:
The Kobe journal of medical sciences vol. 57
Availability: No items available.
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6442.
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6443.
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6444.
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6445.
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6446.
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6447.
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6448.
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6449.
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6450.
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6451.
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6452.
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6453.
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6454.
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6455.
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6456.
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6457.
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6458.
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6459.
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6460.
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