The frequencies of five mutations of the debrisoquine 4-hydroxylase (CYP2D6) gene (mutations D6-A, B, C, 0, and T), corresponding to poor metabolizer (PM) phenotypes, were determined by restriction fragment length polymorphism (RFLP) and polymerase chain reaction (PCR) in 47 patients with Parkinson
β¦ LIBER β¦
Absence of effect of seven functional mutations in the cyp2d6 gene in Parkinson's disease
β Scribed by Oscar Joost; Catherine A. Taylor; Catherine A. Thomas; L. Adrienne Cupples; Marie H. Saint-Hilaire; Robert G. Feldman; Clinton T. Baldwin; Richard H. Myers
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 41 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0885-3185
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