The multiple faces of the ATP1A3-related dystonic movement disorder.
Identifieur interne : 000C09 ( Main/Exploration ); précédent : 000C08; suivant : 000C10The multiple faces of the ATP1A3-related dystonic movement disorder.
Auteurs : Anne Roubergue [France] ; Emmanuel Roze ; Sandrine Vuillaumier-Barrot ; Marie-Joséphine Fontenille ; Aurélie Méneret ; Marie Vidailhet ; Bertrand Fontaine ; Diane Doummar ; Bertrand Philibert ; Florence Riant ; Sophie NicoleSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2013.
English descriptors
- KwdEn :
- Adolescent, Adult, Age of Onset, Child, Preschool, Dystonic Disorders (genetics), Dystonic Disorders (physiopathology), Family, Female, Hemiplegia (genetics), Hemiplegia (physiopathology), Humans, Male, Middle Aged, Mutation (genetics), Parkinson Disease (genetics), Parkinson Disease (physiopathology), Polymerase Chain Reaction, Sodium-Potassium-Exchanging ATPase (genetics), Young Adult.
- MESH :
- chemical , genetics : Sodium-Potassium-Exchanging ATPase.
- genetics : Dystonic Disorders, Hemiplegia, Mutation, Parkinson Disease.
- physiopathology : Dystonic Disorders, Hemiplegia, Parkinson Disease.
- Adolescent, Adult, Age of Onset, Child, Preschool, Family, Female, Humans, Male, Middle Aged, Polymerase Chain Reaction, Young Adult.
DOI: 10.1002/mds.25396
PubMed: 23483595
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 000701
- to stream PubMed, to step Curation: 000670
- to stream PubMed, to step Checkpoint: 000670
- to stream Ncbi, to step Merge: 001096
- to stream Ncbi, to step Curation: 001096
- to stream Ncbi, to step Checkpoint: 001096
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Le document en format XML
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