Rosalind Chuang

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Publication Details

  • Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers.

    Marras C, Schüle B, Schuele B, Munhoz RP, Rogaeva E, Langston JW, Kasten M, Meaney C, Klein C, Wadia PM, Lim SY, Chuang RS, Zadikof C, Steeves T, Prakash KM, de Bie RM, Adeli G, Thomsen T, Johansen KK, Teive HA, Asante A, Reginold W, Lang AE. Neurology. 2011; 77 (4): 325-33

    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.

    PubMedID: 21753163

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