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A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease.
Pihlstrøm L, Blauwendraat C, Cappelletti C, Berge-Seidl V, Langmyhr M, Henriksen SP, van de Berg WDJ, Gibbs JR, Cookson MR; International Parkinson Disease Genomics Consortium; North American Brain Expression Consortium; Singleton AB, Nalls MA, Toft M. Pihlstrøm L, et al. Among authors: cappelletti c. Ann Neurol. 2018 Jul;84(1):117-129. doi: 10.1002/ana.25274. Epub 2018 Aug 26. Ann Neurol. 2018. PMID: 30146727 Free PMC article.
Missense mutations in DYT-TOR1A dystonia.
Iqbal Z, Koht J, Pihlstrøm L, Henriksen SP, Cappelletti C, Russel MB, Norberto de Souza O, Skogseid IM, Toft M. Iqbal Z, et al. Among authors: cappelletti c. Neurol Genet. 2019 Jun 6;5(4):e343. doi: 10.1212/NXG.0000000000000343. eCollection 2019 Aug. Neurol Genet. 2019. PMID: 31321303 Free PMC article. No abstract available.
92 results