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Mutations in SACS cause atypical and late-onset forms of ARSACS
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Document type | Article de périodique (Journal article) – Article de recherche – Journal Article, Research Support, Non-U.S. Gov't |
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Publication date | 2010 |
Language | Anglais |
Journal information | "Neurology" - Vol. 75, no. 13, p. 1181-8 (2010) |
Peer reviewed | yes |
Publisher | Lippincott Williams & Wilkins (Philadelphia) |
issn | 0028-3878 |
e-issn | 1526-632X |
Publication status | Publié |
Affiliations |
UCL
- Cliniques universitaires Saint-Luc UCL - SSS/IONS - Institute of NeuroScience UCL - SSS/DDUV - Institut de Duve UCL - SSS/IONS/NEUR - Clinical Neuroscience UCL - (SLuc) Service de neurologie |
MESH Subject | Young Adult ; Spastic Paraplegia, Hereditary - genetics - pathology ; Phenotype ; Mutation - genetics ; Middle Aged ; Male ; Magnetic Resonance Imaging - methods ; Humans ; Heat-Shock Proteins - genetics ; Female ; DNA Mutational Analysis - methods ; Child ; Adult ; Adolescent |
Links |
Bibliographic reference | Baets, J. ; Van den Bergh, Peter ; Deconinck, T. ; Smets, K. ; Goossens, D. ; et. al. Mutations in SACS cause atypical and late-onset forms of ARSACS. In: Neurology, Vol. 75, no. 13, p. 1181-8 (2010) |
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Permanent URL | http://hdl.handle.net/2078.1/33787 |