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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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