ParkinsonCanadaV1, Main, Exploration, bibRecord, 000184

The Contursi Family 20 Years Later: Intrafamilial Phenotypic Variability of the SNCA p.A53T Mutation.

Identifieur interne : 000184 ( Main/Exploration ); précédent : 000183; suivant : 000185

The Contursi Family 20 Years Later: Intrafamilial Phenotypic Variability of the SNCA p.A53T Mutation.

Auteurs : Lucia Ricciardi [Royaume-Uni] ; Simona Petrucci [Italie] ; Daniela Di Giuda [Italie] ; Laura Serra [Italie] ; Barbara Span [Italie] ; Mariachiara Sensi [Italie] ; Monia Ginevrino [Italie] ; Fabrizio Cocciolillo [Italie] ; Marco Bozzali [Italie] ; Enza Maria Valente [Italie] ; Alfonso Fasano [Canada]

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2016.

RBID : pubmed:26799529

English descriptors

KwdEn :
- Adult, Female, Humans, Male, Middle Aged, Mutation, Parkinson Disease (diagnosis), Parkinson Disease (genetics), Pedigree, Phenotype, alpha-Synuclein (genetics).
MESH :
- chemical , genetics : alpha-Synuclein.
- diagnosis : Parkinson Disease.
- genetics : Parkinson Disease.
- Adult, Female, Humans, Male, Middle Aged, Mutation, Pedigree, Phenotype.

DOI: 10.1002/mds.26549
PubMed: 26799529

Affiliations:

Le document en format XML

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La maladie de Parkinson au Canada (serveur d'exploration)

The Contursi Family 20 Years Later: Intrafamilial Phenotypic Variability of the SNCA p.A53T Mutation.

The Contursi Family 20 Years Later: Intrafamilial Phenotypic Variability of the SNCA p.A53T Mutation.

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

	La maladie de Parkinson au Canada (serveur d'exploration)
	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.