MovDisordV3, Main, Exploration, bibRecord, 002B42

The (−16C > T) substitution in the PLEKHG4 gene is not present among European ADCA patients

Identifieur interne : 002B42 ( Main/Exploration ); précédent : 002B41; suivant : 002B43

The (−16C > T) substitution in the PLEKHG4 gene is not present among European ADCA patients

Auteurs : Claudia Cagnoli [Italie] ; Alessandro Brussino [Italie] ; Eleonora Di Gregorio [Italie] ; Alfredo Brusco [Italie] ; Giovanni Stevanin [France] ; Alexandra Durr [France] ; Alexis Brice [France]

Source :

Movement Disorders [ 0885-3185 ] ; 2007-04-15.

RBID : ISTEX:3FEB49D76636FAC44F81ECB5D6A12A60408DADCF

English descriptors

KwdEn :
- Adolescent, Adult, Aged, Chromosome Aberrations, Chromosome Mapping, Chromosomes, Human, Pair 16, DNA Mutational Analysis, Europe, European Continental Ancestry Group (genetics), Female, Genes, Dominant, Genetics, Population, Guanine Nucleotide Exchange Factors (genetics), Humans, Male, Middle Aged, Spectrin (genetics), Spinocerebellar Ataxias (diagnosis), Spinocerebellar Ataxias (genetics).
MESH :
- chemical , genetics : Guanine Nucleotide Exchange Factors, Spectrin.
- geographic : Europe.
- diagnosis : Spinocerebellar Ataxias.
- genetics : European Continental Ancestry Group, Spinocerebellar Ataxias.
- Adolescent, Adult, Aged, Chromosome Aberrations, Chromosome Mapping, Chromosomes, Human, Pair 16, DNA Mutational Analysis, Female, Genes, Dominant, Genetics, Population, Humans, Male, Middle Aged.

Url:

https://api.istex.fr/document/3FEB49D76636FAC44F81ECB5D6A12A60408DADCF/fulltext/pdf

DOI: 10.1002/mds.21389

Affiliations:

Le document en format XML

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<author><name sortKey="Brussino, Alessandro" sort="Brussino, Alessandro" uniqKey="Brussino A" first="Alessandro" last="Brussino">Alessandro Brussino</name>
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<author><name sortKey="Di Gregorio, Eleonora" sort="Di Gregorio, Eleonora" uniqKey="Di Gregorio E" first="Eleonora" last="Di Gregorio">Eleonora Di Gregorio</name>
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<author><name sortKey="Brusco, Alfredo" sort="Brusco, Alfredo" uniqKey="Brusco A" first="Alfredo" last="Brusco">Alfredo Brusco</name>
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<author><name sortKey="Stevanin, Giovanni" sort="Stevanin, Giovanni" uniqKey="Stevanin G" first="Giovanni" last="Stevanin">Giovanni Stevanin</name>
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<author><name sortKey="Durr, Alexandra" sort="Durr, Alexandra" uniqKey="Durr A" first="Alexandra" last="Durr">Alexandra Durr</name>
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<author><name sortKey="Di Gregorio, Eleonora" sort="Di Gregorio, Eleonora" uniqKey="Di Gregorio E" first="Eleonora" last="Di Gregorio">Eleonora Di Gregorio</name>
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<wicri:regionArea>Department of Genetics Biology and Biochemistry, University of Turin and San Giovanni Battista Hospital, Medical Genetics Unit, Turin</wicri:regionArea>
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<term>Spinocerebellar Ataxias (genetics)</term>
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<term>Aged</term>
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<term>Chromosome Mapping</term>
<term>Chromosomes, Human, Pair 16</term>
<term>DNA Mutational Analysis</term>
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<term>Genes, Dominant</term>
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Movement Disorders (revue)

The (−16C > T) substitution in the PLEKHG4 gene is not present among European ADCA patients

The (−16C > T) substitution in the PLEKHG4 gene is not present among European ADCA patients

Source :

English descriptors

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

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.