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Frequent co-occurrence of the TATA box mutation associated with Gilbert’s syndrome (UGT1A1*28) with other polymorphisms of the UDP-glucuronosyltransferase-1 locus (UGT1A6*2 and UGT1A7*3) in Caucasians and Egyptians
✍ Scribed by Christoph Köhle; Bernd Möhrle; Peter A. Münzel; Matthias Schwab; Dorothee Wernet; Osama A. Badary; Karl Walter Bock
- Book ID
- 113993446
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- English
- Weight
- 131 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0006-2952
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