MovDisordV3, Main, Exploration, bibRecord, 000085

Reply to letter: Novel compound heterozygous mutations in PRKRA cause pure dystonia.

Identifieur interne : 000085 ( Main/Exploration ); précédent : 000084; suivant : 000086

Reply to letter: Novel compound heterozygous mutations in PRKRA cause pure dystonia.

Auteurs : Michael Zech [Allemagne] ; Florian Castrop [Allemagne] ; Bernhard Haslinger [Allemagne] ; Juliane Winkelmann [Allemagne]

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2015.

RBID : pubmed:25914261

English descriptors

KwdEn :
- DNA Copy Number Variations (genetics), Dystonic Disorders (genetics), Exome (genetics), Family Health, Female, Humans, Male, RNA-Binding Proteins (genetics).
MESH :
- chemical , genetics : RNA-Binding Proteins.
- genetics : DNA Copy Number Variations, Dystonic Disorders, Exome.
- Family Health, Female, Humans, Male.

DOI: 10.1002/mds.26233
PubMed: 25914261

Affiliations:

Le document en format XML

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<author><name sortKey="Castrop, Florian" sort="Castrop, Florian" uniqKey="Castrop F" first="Florian" last="Castrop">Florian Castrop</name>
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<term>Humans</term>
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<term>RNA-Binding Proteins (genetics)</term>
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Movement Disorders (revue)

Reply to letter: Novel compound heterozygous mutations in PRKRA cause pure dystonia.

Reply to letter: Novel compound heterozygous mutations in PRKRA cause pure dystonia.

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

Pour générer des pages wiki

	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.