Nuclear and mitochondrial genetics in Parkinson's disease.-Reference-Cited by-同舟云学术

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Nuclear and mitochondrial genetics in Parkinson's disease.

Published:1995-06-01 Issue:6 Volume:32 Page:411-414
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Schapira A H

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference49 articles.

1. Brain dopamine and the syndromes of Parkinson and Huntington;true;J Neurol Sci,1973

2. Twin study of Parkinson disease;Duvoisin, R.C.; Eldridge, R.; Williams, A.; Calne, D.;Neurology,1981

3. Parkinson's disease in 65 pairs of twins and in a set of quadruplets;Ward, C.D.; Duvoisin, R.C.; Ince, S.E.;Neurology,1983

4. Parkinson's disease in a nationwide twin cohort;Martilla, R.J.; Kaprio, J.; Koskenvuo, M.D.; Rinne, U.K.;Neurology,1988

5. Parkinson's disease in twins;Marsden, C.D.;J Neurol Neurosurg Psychiatry,1987

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1. Role of Apolipoproteins and α-Synuclein in Parkinson’s Disease;Journal of Molecular Neuroscience;2017-07-10

2. Mitochondrial Medicine;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

3. Association of long variants of the dopamine D4 receptor exon 3 repeat polymorphism with Parkinson's disease;Clinical Genetics;2008-04-23

4. Genetics of Parkinson's Disease;Annals of the New York Academy of Sciences;2006-01-25

5. Protein oxidation and degradation during aging: Role in skin aging and neurodegeneration;Free Radical Research;2006-01

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