Hagenah, J.

mutation carrier family disease parkinson 1441c mutation carriers c .1366c patient neurology .1366c t mutation 1 mrna levels analysis haplotype study parkinsonism level parkinson disease substitution lrrk 2 department 1 mutations 1366 t allele university allele genomic dna genomic italian 1 exon 5–6 www.neurology.org feature sample table early-onset signal kinase 1 gene haplotype analysis control ywhaz pathology figure symptom nonsense-mediated mrna decay 1 mrna level 1366 t signal ϯ sd age klein lrrk 2 mutations parkinson disease k german transcript effect phenotypic variability onset information microsatellite .4321c exon 7–8 part 2 german family assay control genes phase germany incidence status population guest expression neurogenetic institute article downloaded genet domain disorder sequencing lrrk 2 protein