SMPD1 mutations and Parkinson disease

Affiliations

¹ Department of Nursing, Faculty of Social Welfare and Health Sciences, University of Haifa, Haifa, Israel.
² The Simon Winter Institute for Human Genetics, Bnei Zion Medical Center, Haifa, Israel; The Ruth and Bruce Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel.
³ The Ruth and Bruce Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel; Department of Neurology and the Cognitive Neurology Institute, Rambam Health Care Campus, Haifa, Israel.
⁴ Institute of Human Genetics, Rambam Health Care Campus, Haifa, Israel.
⁵ Department of Neurology and the Cognitive Neurology Institute, Rambam Health Care Campus, Haifa, Israel.
⁶ The Simon Winter Institute for Human Genetics, Bnei Zion Medical Center, Haifa, Israel; Institute of Human Genetics, Rambam Health Care Campus, Haifa, Israel. Electronic address: rgershoni@rambam.health.gov.il.

Comment

E Dagan et al. Parkinsonism Relat Disord. 2015 Oct.

. 2015 Oct;21(10):1296-7.

doi: 10.1016/j.parkreldis.2015.08.019. Epub 2015 Aug 20.

¹ Department of Nursing, Faculty of Social Welfare and Health Sciences, University of Haifa, Haifa, Israel.
² The Simon Winter Institute for Human Genetics, Bnei Zion Medical Center, Haifa, Israel; The Ruth and Bruce Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel.
³ The Ruth and Bruce Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel; Department of Neurology and the Cognitive Neurology Institute, Rambam Health Care Campus, Haifa, Israel.
⁴ Institute of Human Genetics, Rambam Health Care Campus, Haifa, Israel.
⁵ Department of Neurology and the Cognitive Neurology Institute, Rambam Health Care Campus, Haifa, Israel.
⁶ The Simon Winter Institute for Human Genetics, Bnei Zion Medical Center, Haifa, Israel; Institute of Human Genetics, Rambam Health Care Campus, Haifa, Israel. Electronic address: rgershoni@rambam.health.gov.il.

No abstract available

Keywords: GBA; Gaucher disease; Niemann-Pick disease; Parkinson's disease; SMPD1.

Comment on

The contribution of Niemann-Pick SMPD1 mutations to Parkinson disease in Ashkenazi Jews.
Dagan E, Schlesinger I, Ayoub M, Mory A, Nassar M, Kurolap A, Peretz-Aharon J, Gershoni-Baruch R. Dagan E, et al. Parkinsonism Relat Disord. 2015 Sep;21(9):1067-71. doi: 10.1016/j.parkreldis.2015.06.016. Epub 2015 Jun 19. Parkinsonism Relat Disord. 2015. PMID: 26169695
The emerging role of SMPD1 mutations in Parkinson's disease: Implications for future studies.
Gan-Or Z, Orr-Urtreger A, Alcalay RN, Bressman S, Giladi N, Rouleau GA. Gan-Or Z, et al. Parkinsonism Relat Disord. 2015 Oct;21(10):1294-5. doi: 10.1016/j.parkreldis.2015.08.018. Epub 2015 Aug 20. Parkinsonism Relat Disord. 2015. PMID: 26320887