La maladie de Parkinson en France (serveur d'exploration)

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Genetics of movement disorders.

Identifieur interne : 001451 ( PubMed/Checkpoint ); précédent : 001450; suivant : 001452

Genetics of movement disorders.

Auteurs : A. Dürr [France] ; A. Brice

Source :

RBID : pubmed:8858187

English descriptors

Abstract

Trinucleotide repeat expansions or unstable mutations are the cause of a growing number of hereditary movement disorders, especially inherited ataxias. Diagnostic practice as well as disease classifications have altered accordingly. Genes responsible for "Parkinsonian plus' syndromes and episodic movement disorders have also been recently mapped.

PubMed: 8858187


Affiliations:


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pubmed:8858187

Le document en format XML

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   |type=    RBID
   |clé=     pubmed:8858187
   |texte=   Genetics of movement disorders.
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