Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers

OBJECTIVES: Using a family study design, we describe the motor and nonmotor phenotype in probands with LRRK2 G2019S mutations and family members and compare these individuals to patients with idiopathic Parkinson disease (iPD) and unrelated controls. METHODS: Probands with G2019S mutations and their...

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Hlavní autoři: Marras, C., Schuele, B., Munhoz, R.P., Rogaeva, E., Langston, J.W., Kasten, M., Meaney, C., Klein, C., Wadia, P.M., Lim, S.-Y., Chuang, R.S.-I., Zadikof, C., Steeves, T., Prakash, K.M., de Bie, R.M.A., Adeli, G., Thomsen, T., Johansen, K.K., Teive, H.A., Asante, A., Reginold, W., Lang, A.E.
Médium: Artigo
Jazyk:Inglês
Vydáno: Lippincott Williams & Wilkins 2011
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3140802/
https://ncbi.nlm.nih.gov/pubmed/21753163
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e318227042d
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