MovDisordV3, PascalFrancis, Checkpoint, bibRecord, 003515

CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy

Identifieur interne : 003515 ( PascalFrancis/Checkpoint ); précédent : 003514; suivant : 003516

CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy

Auteurs : V. Plante-Bordeneuve [Royaume-Uni] ; O. Bandmann ; G. Wenning ; N. P. Quinn ; S. E. Daniel ; A. E. Harding

Source :

Movement disorders [ 0885-3185 ] ; 1995.

RBID : Pascal:95-0363321

Descripteurs français

Pascal (Inist)
- Parkinson maladie, Polymorphisme, Gène, Cytochrome P450, Débrisoquine, Hydroxylase, Etude comparative, Exploration, Homme, CYP2D6, Atrophie multisystématisée.
Wicri :
- topic : Homme.

English descriptors

KwdEn :
- Comparative study, Cytochrome P450, Exploration, Gene, Human, Hydroxylase, Multiple system atrophy, Parkinson disease, Polymorphism.

Affiliations:

Royaume-Uni

Links toward previous steps (curation, corpus...)

to stream PascalFrancis, to step Corpus: 003499
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Links to Exploration step

Pascal:95-0363321

Le document en format XML

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<s2>London WC1N 3BG</s2>
<s3>GBR</s3>
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<country>Royaume-Uni</country>
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<author><name sortKey="Quinn, N P" sort="Quinn, N P" uniqKey="Quinn N" first="N. P." last="Quinn">N. P. Quinn</name>
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<author><name sortKey="Daniel, S E" sort="Daniel, S E" uniqKey="Daniel S" first="S. E." last="Daniel">S. E. Daniel</name>
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<author><name sortKey="Harding, A E" sort="Harding, A E" uniqKey="Harding A" first="A. E." last="Harding">A. E. Harding</name>
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	Movement Disorders (revue)
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Movement Disorders (revue)

CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy

CYP2D6-debrisoquine hydroxylase gene polymorphism in multiple system atrophy

Source :

Descripteurs français

English descriptors

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri