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42. A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion. Dogu O; Johnson J; Hernandez D; Hanson M; Hardy J; Apaydin H; Özekmekçi S; Sevim S; Gwinn-Hardy K; Singleton A Mov Disord; 2004 Jul; 19(7):812-816. PubMed ID: 15254940 [TBL] [Abstract][Full Text] [Related]
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48. New mutation (R42P) of the parkin gene in the ubiquitinlike domain associated with parkinsonism. Terreni L; Calabrese E; Calella AM; Forloni G; Mariani C Neurology; 2001 Feb; 56(4):463-6. PubMed ID: 11222788 [TBL] [Abstract][Full Text] [Related]
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56. Homozygous deletion mutation of the parkin gene in patients with atypical parkinsonism. Kuroda Y; Mitsui T; Akaike M; Azuma H; Matsumoto T J Neurol Neurosurg Psychiatry; 2001 Aug; 71(2):231-4. PubMed ID: 11459900 [TBL] [Abstract][Full Text] [Related]
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