Division of Molecular Biology & Human Genetics
?Parkinson's Disease
2010 Publications
Bardien S, Marsberg A, Keyser R, Lombard D, Lesage S, Brice A, Carr J. LRRK2 G2019S mutation: frequency and haplotype data in South African Parkinson's disease patients. Journal of Neural Transmission (Vienna). 2010: 117(7):847-53. DOI: 10.1007/s00702-010-0423-6. Epub 2010. PMID: 20544233
Keyser RJ, Lesage S, Brice A, Carr J, Bardien S. Assessing the prevalence of PINK1 genetic variants in South African patients diagnosed with early- and late-onset Parkinson's disease. Biochemical and Biophysical Research Communications. 2010 Jul: 398(1):125-9. DOI: 10.1016/j.bbrc.2010.06.049. Epub 2010. PMID: 20558144
Lesage S, Patin E, Condroyer C, Leutenegger AL, Lohmann E, Giladi N, Bar-Shira A, Belarbi S, Hecham N, Pollak P, Ouvrard-Hernandez AM, Bardien S, Carr J, Benhassine T, Tomiyama H, Pirkevi C, Hamadouche T, Cazeneuve C, Basak AN, Hattori N, Dürr A, Tazir M, Orr-Urtreger A, Quintana-Murci L, Brice A; French Parkinson's Disease Genetics Study Group. Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans. Human Molecular Genetics. 2010: 19(10):1998-2004. DOI: 10.1093/hmg/ddq081. Epub 2010. PMID: 20197411
