(Q44828247)

6 December 2017

title

Interaction between GSTM1-null and CYP2D6-deficient alleles in the pathogenesis of Parkinson's disease (English)

1 reference

6 December 2017

O Santt

1

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6 December 2017

H Baranova

2

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6 December 2017

E Albuisson

3

1 reference

6 December 2017

Y-J Bignon

4

1 reference

6 December 2017

G Lucotte

5

1 reference

6 December 2017

publication date

1 April 2004

1 reference

European Journal of Neurology

6 December 2017

published in

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6 December 2017

volume

11

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6 December 2017

issue

4

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6 December 2017

page(s)

247-251

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Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease

6 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2003.00756.X

Metabolism of MPTP by cytochrome P4502D6 and the demonstration of 2D6 mRNA in human foetal and adult brain by in situ hybridization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2003.00756.X

Identification of the primary gene defect at the cytochrome P450 CYP2D locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2003.00756.X

Mutation frequencies of the cytochrome CYP2D6 gene in Parkinson disease patients and in families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2003.00756.X

Cellular localization and regional distribution of CYP2D6 mRNA and protein expression in human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2003.00756.X

Determination of glutathione S-transferase mu and theta polymorphisms in neurological disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.2003.00756.X

10.1046/J.1468-1331.2003.00756.X

21 January 2018

Identifiers

DOI

1 reference

6 December 2017

1 reference