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Point mutations in exon 1 of theNR4A2gene are not a major cause of familial Parkinson′s disease

✍ Scribed by Alexander Zimprich; Friedrich Asmus; Petra Leitner; Mirna Castro; Benjamin Bereznai; Nikolaus Homann; Erwin Ott; A.WijnandF. Rutgers; Gyri Wieditz; Claudia Trenkwalder; Thomas Gasser


Publisher
Springer
Year
2003
Tongue
English
Weight
106 KB
Volume
4
Category
Article
ISSN
1364-6745

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Mutations in LRRK2 other than G2019S are
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## Abstract A total of 956 individuals with Parkinson's disease (PD) from 430 multiplex PD pedigrees were screened for 12 previously reported, pathogenic __LRRK2__ mutations: R793M, L1114L, I1371V, R1441C, R1441G, R1441H, Y1699C, M1869T, I2012T, I2020T, G2385R, and IVS31 +3G>A. Previous screening i