Debrisoquine hydroxylase gene polymorphism in familial Parkinson's disease.

Author:

Plante-Bordeneuve V,Davis M B,Maraganore D M,Marsden C D,Harding A E

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Reference18 articles.

1. Parkinson's disease in 65 pairs of twins and in a set of quadruplets;Ward, C.D.; Duvoisin, R.C.; Ince, S.E.; Nutt, J.D.; Eldridge, R.; Calne, D.B.;Neurology,1983

2. A large kindred with autosomal dominant Parkinson's disease;Golbe, L.I.; Di Iorio, G.; Bonavita, V.; Miller, D.C.; Duvoisin, R.C.;Ann Neurol,1990

3. Parkinson's disease in twins studied with "8F-DOPA and positron emission tomography;Burn, D.J.; Mark, M.H.; Playford, E.D.;Neurology,1992

4. New insights into the cause of Parkinson's disease;Jenner, P.; Schapira, A.H.V.; Marsden, C.D.;Neurology,1992

5. Ecogenetics of Parkinson's disease: 4-hydroxylation of debrisoquine;Barbeau, A.; Cloutier, T.; Roy, M.; Plasse, L.; Paris, S.; Poirier, J.;Lancet,1985

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