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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, P; Lohman, E; Benhassine, T; Ysmail-Dahlouk, F; Dürr, A; Tazir, M; Brice, A.
Affiliation
  • Lesage S; INSERM UMR 679 (former U289), Hôpital de la Salpêtrière, Paris Cedex 13, France.
Neurology ; 71(19): 1550-2, 2008 Nov 04.
Article in En | MEDLINE | ID: mdl-18981379
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease / Protein Serine-Threonine Kinases / Point Mutation / Dyskinesias Limits: Adolescent / Adult / Aged / Aged80 / Child / Female / Humans / Male / Middle aged Country/Region as subject: Africa Language: En Journal: Neurology Year: 2008 Document type: Article Affiliation country: Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease / Protein Serine-Threonine Kinases / Point Mutation / Dyskinesias Limits: Adolescent / Adult / Aged / Aged80 / Child / Female / Humans / Male / Middle aged Country/Region as subject: Africa Language: En Journal: Neurology Year: 2008 Document type: Article Affiliation country: Country of publication: