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4. Genomic instability in the PARK2 locus is associated with Parkinson's disease. Ambroziak W; Koziorowski D; Duszyc K; Górka-Skoczylas P; Potulska-Chromik A; Sławek J; Hoffman-Zacharska D J Appl Genet; 2015 Nov; 56(4):451-461. PubMed ID: 25833766 [TBL] [Abstract][Full Text] [Related]
5. Low frequency of the PARK2 gene mutations in Polish patients with the early-onset form of Parkinson disease. Koziorowski D; Hoffman-Zacharska D; Sławek J; Szirkowiec W; Janik P; Bal J; Friedman A Parkinsonism Relat Disord; 2010 Feb; 16(2):136-8. PubMed ID: 19628420 [TBL] [Abstract][Full Text] [Related]
6. High frequency of Parkin exon rearrangements in Mexican-mestizo patients with early-onset Parkinson's disease. Guerrero Camacho JL; Monroy Jaramillo N; Yescas Gómez P; Rodríguez Violante M; Boll Woehrlen C; Alonso Vilatela ME; López López M Mov Disord; 2012 Jul; 27(8):1047-51. PubMed ID: 22777964 [TBL] [Abstract][Full Text] [Related]
7. Variable PARK2 Mutations Cause Early-Onset Parkinson's Disease in a Small Restricted Population. Ben-Shachar S; Afawi Z; Masalha R; Badarny S; Neiman T; Pavzner D; Bar-Shira A; Orr-Urtreger A J Mol Neurosci; 2017 Oct; 63(2):216-222. PubMed ID: 28913705 [TBL] [Abstract][Full Text] [Related]
8. Han Chinese family with early-onset Parkinson's disease carries novel compound heterozygous mutations in the PARK2 gene. Huang T; Gao CY; Wu L; Gong PY; Wang JZ; Tian YY; Zhang YD Brain Behav; 2019 Sep; 9(9):e01372. PubMed ID: 31386307 [TBL] [Abstract][Full Text] [Related]
9. Exonic rearrangements in the known Parkinson's disease-causing genes are a rare cause of the disease in South African patients. van der Merwe C; Carr J; Glanzmann B; Bardien S Neurosci Lett; 2016 Apr; 619():168-71. PubMed ID: 27001088 [TBL] [Abstract][Full Text] [Related]
10. PARK2 gene mutations in early onset Parkinson's disease patients of South India. Padmaja MV; Jayaraman M; Srinivasan AV; Srisailapathy CR; Ramesh A Neurosci Lett; 2012 Aug; 523(2):145-7. PubMed ID: 22766139 [TBL] [Abstract][Full Text] [Related]
11. Occurrence of PARK2 mutations in a never-smoker population with Parkinson's disease in North India. Prabhakar S; Vinish M; Das CP; Anand A Neuroepidemiology; 2010 Aug; 35(2):152-9. PubMed ID: 20571283 [TBL] [Abstract][Full Text] [Related]
12. Phase analysis identifies compound heterozygous deletions of the PARK2 gene in patients with early-onset Parkinson disease. Kim SY; Seong MW; Jeon BS; Kim SY; Ko HS; Kim JY; Park SS Clin Genet; 2012 Jul; 82(1):77-82. PubMed ID: 21534944 [TBL] [Abstract][Full Text] [Related]
13. Parkin mutations in familial and sporadic Parkinson's disease among Indians. Chaudhary S; Behari M; Dihana M; Swaminath PV; Govindappa ST; Jayaram S; Goyal V; Maitra A; Muthane UB; Juyal RC; Thelma BK Parkinsonism Relat Disord; 2006 May; 12(4):239-45. PubMed ID: 16500134 [TBL] [Abstract][Full Text] [Related]
15. Prevalence of parkin gene mutations and variations in idiopathic Parkinson's disease. Sinha R; Racette B; Perlmutter JS; Parsian A Parkinsonism Relat Disord; 2005 Sep; 11(6):341-7. PubMed ID: 16019250 [TBL] [Abstract][Full Text] [Related]
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17. Incidence of mutations in the PARK2, PINK1, PARK7 genes in Polish early-onset Parkinson disease patients. Koziorowski D; Hoffman-Zacharska D; Sławek J; Jamrozik Z; Janik P; Potulska-Chromik A; Roszmann A; Tataj R; Bal J; Friedman A Neurol Neurochir Pol; 2013; 47(4):319-24. PubMed ID: 23986421 [TBL] [Abstract][Full Text] [Related]
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19. Analysis of Exon Dosage Using Multiplex Ligation-Dependent Probe Amplification in Chinese Patients with Early-Onset Parkinson's Disease. Lin Y; Zeng YF; Cai NQ; Lin XZ; Wang N; He J Eur Neurol; 2019; 81(5-6):246-253. PubMed ID: 31618739 [TBL] [Abstract][Full Text] [Related]
20. Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease. Jankovic MZ; Dobricic V; Kresojevic N; Markovic V; Petrovic I; Svetel M; Pekmezovic T; Novakovic I; Kostic V J Neurol Sci; 2018 Oct; 393():27-30. PubMed ID: 30099245 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]