Title: The <scp>L444P</scp><i><scp>GBA</scp></i> mutation is associated with early‐onset Parkinson's disease in Mexican Mestizos
Abstract: Clinical GeneticsVolume 84, Issue 4 p. 386-387 LETTER TO THE EDITOR The L444P GBA mutation is associated with early-onset Parkinson's disease in Mexican Mestizos M de L González-del Rincón, M de L González-del Rincón Neurogenetics DepartmentSearch for more papers by this authorN Monroy Jaramillo, N Monroy Jaramillo Neurogenetics DepartmentSearch for more papers by this authorAI Suárez Martínez, AI Suárez Martínez Neurogenetics DepartmentSearch for more papers by this authorP Yescas Gómez, P Yescas Gómez Neurogenetics DepartmentSearch for more papers by this authorMC Boll Woehrlen, MC Boll Woehrlen Clinic Research Laboratory, National Institute of Neurology and Neurosurgery (NINN) "Manuel Velasco Suárez", Mexico City, MexicoSearch for more papers by this authorM López López, M López López Biological Systems Department, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, MexicoSearch for more papers by this authorME Alonso Vilatela, Corresponding Author ME Alonso Vilatela Neurogenetics Department Correspondence: María Elisa Alonso, MD Neurogenetics Department National Institute of Neurology and Neurosurgery "Manuel Velasco Suárez" Insurgentes Sur 3877, Col. La Fama, Tlalpan, 12269 Mexico City Mexico. Tel.: +52-55-56063822 fax.: +52-55-54240808 e-mail: [email protected]Search for more papers by this author M de L González-del Rincón, M de L González-del Rincón Neurogenetics DepartmentSearch for more papers by this authorN Monroy Jaramillo, N Monroy Jaramillo Neurogenetics DepartmentSearch for more papers by this authorAI Suárez Martínez, AI Suárez Martínez Neurogenetics DepartmentSearch for more papers by this authorP Yescas Gómez, P Yescas Gómez Neurogenetics DepartmentSearch for more papers by this authorMC Boll Woehrlen, MC Boll Woehrlen Clinic Research Laboratory, National Institute of Neurology and Neurosurgery (NINN) "Manuel Velasco Suárez", Mexico City, MexicoSearch for more papers by this authorM López López, M López López Biological Systems Department, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, MexicoSearch for more papers by this authorME Alonso Vilatela, Corresponding Author ME Alonso Vilatela Neurogenetics Department Correspondence: María Elisa Alonso, MD Neurogenetics Department National Institute of Neurology and Neurosurgery "Manuel Velasco Suárez" Insurgentes Sur 3877, Col. La Fama, Tlalpan, 12269 Mexico City Mexico. Tel.: +52-55-56063822 fax.: +52-55-54240808 e-mail: [email protected]Search for more papers by this author First published: 01 March 2013 https://doi.org/10.1111/cge.12084Citations: 15Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References 1Lesage S, Brice A. Role of Mendelian genes in "sporadic" Parkinson's disease. Parkinsonism Relat Disord 2012: 18S1: S66–S70. 2Sidransky E, Nalls MA, Aasly JO et al. Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. N Engl J Med 2009: 361 (17): 1651–1661. 3Newmann J, Bras J, Deas E et al. Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease. Brain 2009: 132: 1783–1794. 4Bras JM, Singleton A. Genetic susceptibility in Parkinson's disease. Biochim Biophys Acta 2009: 1792: 597–603. 5Aharon-Peretz J, Rosenbaum H, Gershoni-Baruch R. Mutations in glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews. N Engl J Med 2004: 351 (19): 1972–1977. 6Anheim M, Elbaz A, Lesage S et al. Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers. Neurology 2012: 78: 417–420. 7Gan-Or Z, Giladi N, Orr-Urtreger A. Differential phenotype in Parkinson's disease patients with severe versus mild GBA mutations. Brain 2009: 132 (Pt 10): e125. 8Brockmann K, Srulijes K, Hauser AK, Schulte C. GBA associated PD presents with nonmotor characteristics. Neurology 2011: 77: 276–280. Citing Literature Volume84, Issue4October 2013Pages 386-387 ReferencesRelatedInformation