MovDisordV3, PubMed, Checkpoint, bibRecord, 000279

DYT2 Revealed: Hippocalcin Mutations Cause Autosomal-Recessive Isolated Dystonia.

Identifieur interne : 000279 ( PubMed/Checkpoint ); précédent : 000278; suivant : 000280

DYT2 Revealed: Hippocalcin Mutations Cause Autosomal-Recessive Isolated Dystonia.

Auteurs : Roberto Erro [Royaume-Uni] ; Christine Klein [Allemagne]

Source :

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

RBID : pubmed:26094611
DOI: 10.1002/mds.26280
PubMed: 26094611

Affiliations:

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pubmed:26094611

Le document en format XML

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<AffiliationInfo><Affiliation>Dipartimento di Scienze Neurologiche e del Movimento, Università di Verona, Verona, Italy.</Affiliation>
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   |texte=   DYT2 Revealed: Hippocalcin Mutations Cause Autosomal-Recessive Isolated Dystonia.
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	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.

Movement Disorders (revue)

DYT2 Revealed: Hippocalcin Mutations Cause Autosomal-Recessive Isolated Dystonia.

DYT2 Revealed: Hippocalcin Mutations Cause Autosomal-Recessive Isolated Dystonia.

Source :

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

Pour générer des pages wiki