K. Morike

Debrisoquine/sparteine hydroxylation genotype and phenotype: analysis of common mutations and alleles of CYP2D6 in a European population.

M. Eichelbaum, U. Meyer, A. Gaedigk, 1991, DNA and cell biology.

Ethnic variability in the allelic distribution of human aryl hydrocarbon receptor codon 554 and assessment of variant receptor function in vitro.

R. Tyndale, E. Sellers, U. Meyer, 2001, Pharmacogenetics.

Acetylation pharmacogenetics. The slow acetylator phenotype is caused by decreased or absent arylamine N-acetyltransferase in human liver.

D. Grant, M. Eichelbaum, U. Meyer, 1990, The Journal of clinical investigation.