A nonsense mutation in the cytochrome P450 CYP2D6 gene identified in a Caucasian with an enzyme deficiency
- 1 November 1995
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 96 (5) , 601-603
- https://doi.org/10.1007/bf00197419
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- A missense mutation in exon 6 of the CYP2D6 gene leading to a histidine 324 to proline exchange is associated with the poor metabolizer phenotype of sparteineNaunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1994
- Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotypeHuman Molecular Genetics, 1994
- Poor metabolisers of nicotine and CYP2D6 polymorphismThe Lancet, 1994
- Pharmacogenetic Phenotyping and GenotypingClinical Pharmacokinetics, 1994
- Genetic polymorphism of cytochrome P450 CYP2D6 in Zimbabwean populationPharmacogenetics, 1993
- Relationship between personality and debrisoquine hydroxylation capacityActa Psychiatrica Scandinavica, 1993
- Metabolic polymorphismsPharmacology & Therapeutics, 1993
- Mutant debrisoquine hydroxylation genes in Parkinson's diseaseThe Lancet, 1992
- A tobacco smoke-derived nitrosamine, 4-(methytnitrosamino)-1-(3-pyridyl)-1-butanone, is activated by multiple human cytocbrome P450s including the polymorphic human cytochrome P4502D6Carcinogenesis: Integrative Cancer Research, 1991
- Genotyping of poor metabolisers of debrisoquine by allele-specific PCR amplificationThe Lancet, 1990