| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6283490 | Neuroscience Letters | 2013 | 5 Pages |
Abstract
⺠The overall prevalence of LRRK2 G2019S mutation in this series was 5.45%. ⺠No R1441G substitution was identified in this series. ⺠PD in LRRK2 mutations carriers was indistinguishable for the idiopathic PD. ⺠Systemic imnuno-mediated disorders were identified in 2 of 3 G2019S carriers.
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Authors
Emilia Mabel Gatto, Virginia Parisi, Daniela Paola Converso, Juan José Poderoso, MarÃa Cecilia Carreras, José Felix MartÃ-Massó, Coro Paisán-Ruiz,