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1007 GILBERT'S SYNDROME AND HYPERBILIRUBINEMIA IN PROTEASE INHIBITOR THERAPY – AN EXTENDED HAPLOTYPE OF GENETIC VARIANTS INCREASES RISK IN INDINAVIR TREATMENT

✍ Scribed by Lankisch, T.; Behrens, G.; Ehmer, U.; Möbius, U.; Rockstroh, J.; Wehmeier, M.; Kalthoff, S.; Freiberg, N.; Manns, M.; Schmidt, R.; Strassburg, C.


Book ID
122893839
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
51 KB
Volume
50
Category
Article
ISSN
0168-8278

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