Cerebrospinal fluid biomarkers and clinical features in leucine-rich repeat kinase 2 (LRRK2) mutation carriers.
Identifieur interne : 000416 ( Main/Exploration ); précédent : 000415; suivant : 000417Cerebrospinal fluid biomarkers and clinical features in leucine-rich repeat kinase 2 (LRRK2) mutation carriers.
Auteurs : Dolores Vilas [Espagne] ; Leslie M. Shaw [États-Unis] ; Peggy Taylor [États-Unis] ; Daniela Berg [Allemagne] ; Kathrin Brockmann [Allemagne] ; Jan Aasly [Norvège] ; Connie Marras [Canada] ; Claustre Pont-Sunyer [Espagne] ; José Ríos [Espagne] ; Ken Marek [États-Unis] ; Eduardo Tolosa [Espagne]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2016.
Abstract
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the most common cause of inherited Parkinson's disease (PD). Nonmanifesting carriers of LRRK2 mutations are at high risk for developing PD. Information available on cerebrospinal fluid (CSF) biomarkers in LRRK2 carriers remains preliminary.
DOI: 10.1002/mds.26591
PubMed: 27041685
Affiliations:
- Allemagne, Canada, Espagne, Norvège, États-Unis
- Bade-Wurtemberg, Catalogne, Connecticut, District de Tübingen, Massachusetts, Pennsylvanie, Trøndelag
- Barcelone, Trondheim, Tübingen
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the most common cause of inherited Parkinson's disease (PD). Nonmanifesting carriers of LRRK2 mutations are at high risk for developing PD. Information available on cerebrospinal fluid (CSF) biomarkers in LRRK2 carriers remains preliminary.</div>
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