Oromandibular and lingual dystonia associated with spinocerebellar ataxia type 8
Identifieur interne : 003960 ( Ncbi/Checkpoint ); précédent : 003959; suivant : 003961Oromandibular and lingual dystonia associated with spinocerebellar ataxia type 8
Auteurs : Mwiza Ushe [États-Unis] ; Joel S. Perlmutter [États-Unis]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2012.
English descriptors
- KwdEn :
- MESH :
- complications : Spinocerebellar Degenerations.
- diagnosis : Dystonia.
- etiology : Dystonia.
- genetics : Dystonia, Genetic Predisposition to Disease, Spinocerebellar Degenerations.
- Atrophy, Female, Humans, Middle Aged.
Url:
DOI: 10.1002/mds.25295
PubMed: 23283653
PubMed Central: 3539208
Affiliations:
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- to stream PubMed, to step Curation: 000B21
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PMC:3539208Le document en format XML
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<term>Genetic Predisposition to Disease (genetics)</term>
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