Search Results - Klein, Christine

Author correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2) by M. Lange, Lara, Illarionova, Anastasia, Tan, Ai-Huey, Sarmiento, Ignacio J. Keller, Klein, Christine, Mohamed, Wael Mohamed Yousef

Get full text
Get full text
Get full text
Get full text

The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population by Lange, Lara M., Levine, Kristin, Fox, Susan H., Marras, Connie, Ahmed, Nazish, Kuznetsov, Nicole, Vitale, Dan, Iwaki, Hirotaka, Lohmann, Katja, Marsili, Luca, Espay, Alberto J., Bauer, Peter, Beetz, Christian, Martin, Jessica, Factor, Stewart A., Higginbotham, Lenora A., Chen, Honglei, Leonard, Hampton, Nalls, Mike A., Mencacci, Niccolo E., Morris, Huw R., Singleton, Andrew B., Klein, Christine, Blauwendraat, Cornelis, Fang, Zih-Hua, Mohamed, Wael Mohamed Yousef

Get full text
Get full text
Get full text
Get full text
Get full text

Tackling a disease on a global scale, the Global Parkinson’s Genetics Program, GP2: a new generation of opportunities by Blauwendraat, Cornelis, Noyce, Alastair J., Mata, Ignacio F., Screven, Laurel A., Solle, J., Dumanis, Sonya B., Riley, Ekemini A., Perinan, Maria Teresa, Okubadejo, Njideka, Klein, Christine, Morris, Huw R., Singleton, Andrew B., Mohamed, Wael Mohamed Yousef

Get full text
Get full text
Get full text
Get full text
Get full text