Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

Lesage, S.; Belarbi, S.; Troiano, A.; Condroyer, C.; Hecham, N.; Pollak, Pierre; Lohman, E.; Benhassine, T.; Ysmail-Dahlouk, F.; Durr, A.; Tazir, M.; Brice, A.

doi:10.1212/01.wnl.0000338460.89796.06

Scientific article

English

Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

ContributorsLesage, S.; Belarbi, S.; Troiano, A.; Condroyer, C.; Hecham, N.; Pollak, Pierre; Lohman, E.; Benhassine, T.; Ysmail-Dahlouk, F.; Durr, A.; Tazir, M.; Brice, A.

Published inNeurology, vol. 71, no. 19, p. 1550-1552

Publication date2008

Keywords

Adolescent
Adult
Africa, Northern
Aged
Aged, 80 and over
Child
Dyskinesias/*genetics
Female
Humans
Male
Middle Aged
Parkinson Disease/*genetics/physiopathology
*Point Mutation
Protein-Serine-Threonine Kinases/*genetics

Affiliation entities

Faculté de médecine / Section de médecine clinique / Département des neurosciences cliniques

Research groups

Maladie de Parkinson (911)

Citation (ISO format)

LESAGE, S. et al. Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease? In: Neurology, 2008, vol. 71, n° 19, p. 1550–1552. doi: 10.1212/01.wnl.0000338460.89796.06

Article

Identifiers

PID : unige:19190
DOI : 10.1212/01.wnl.0000338460.89796.06
PMID : 18981379

Additional URL for this publicationhttp://www.neurology.org/content/71/19/1550.full.pdf

Journal ISSN0028-3878

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Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

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