Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansion
Identifieur interne : 005155 ( Main/Exploration ); précédent : 005154; suivant : 005156Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansion
Auteurs : M. G. Hanna [Royaume-Uni] ; M. B. Davis [Royaume-Uni] ; M. G. Sweeney [Royaume-Uni] ; M. Noursadeghi [Royaume-Uni] ; C. J. Ellis [Royaume-Uni] ; P. Elliot [Royaume-Uni] ; N. W. Wood [Royaume-Uni] ; C. D. Marsden [Royaume-Uni]Source :
- Movement disorders [ 0885-3185 ] ; 1998.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Enfant.
English descriptors
- KwdEn :
Affiliations:
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Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansion</title>
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<series><title level="j" type="main">Movement disorders</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Case study</term>
<term>Child</term>
<term>Chorea</term>
<term>Clinical form</term>
<term>Diagnosis</term>
<term>Friedreich ataxia</term>
<term>Gene</term>
<term>Generalized</term>
<term>Genetic determinism</term>
<term>Genotype</term>
<term>Homozygosity</term>
<term>Male</term>
<term>Repeated sequence</term>
<term>Trinucleotide</term>
<term>Young adult</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Hérédodégénérescence spinocérébelleuse Friedreich</term>
<term>Chorée syndrome</term>
<term>Généralisé</term>
<term>Génotype</term>
<term>Homozygotie</term>
<term>Trinucléotide</term>
<term>Séquence répétée</term>
<term>Gène</term>
<term>Etude cas</term>
<term>Diagnostic</term>
<term>Déterminisme génétique</term>
<term>Forme clinique</term>
<term>Adulte jeune</term>
<term>Enfant</term>
<term>Mâle</term>
<term>Frataxine</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Enfant</term>
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