References
Sazci A, Ergul E, Bayulkem K. Association of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene in patients with essential tremor in Turkey. Mov Disord 2004, 19: 1472–1476.
Deng H, Wang P, Jankovic J. The genetics of Parkinson disease. Ageing Res Rev 2017, 42: 72–85.
Pahwa R, Lyons KE. Essential tremor: differential diagnosis and current therapy. Am J Med 2003, 115: 134–142.
Chen JJ, Swope DM. Essential tremor: diagnosis and treatment. Pharmacotherapy 2003, 23: 1105–1122.
Gulcher JR, Jonsson P, Kong A, Kristjansson K, Frigge ML, Karason A, et al. Mapping of a familial essential tremor gene, FET1, to chromosome 3q13. Nat Genet 1997, 17: 84–87.
Higgins JJ, Pho LT, Nee LE. A gene (ETM) for essential tremor maps to chromosome 2p22-p25. Mov Disord 1997, 12: 859–864.
Shatunov A, Sambuughin N, Jankovic J, Elble R, Lee HS, Singleton AB, et al. Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23. Brain 2006, 129(Pt 9): 2318–2331.
Louis ED, Yi H, Erickson-Davis C, Vonsattlel JP, Faust PL. Structural study of Purkinje cell axonal torpedoes in essential tremor. Neurosci Lett 2009, 450: 287–291.
Fang W, Chen H, Wang H, Zhang H, Puneet M, Liu M, et al. Essential tremor is associated with disruption of functional connectivity in the ventral intermediate nucleus- motor cortex-cerebellum circuit. Hum Brain Mapp 2016, 37: 165–178.
Stefansson H, Steinberg S, Petursson H, Gustafsson O, Gudjonsdottir IH, Jonsdottir GA, et al. Variant in the sequence of the LINGO1 gene confers risk of essential tremor. Nat Genet 2009, 41(3): 277–279. Erratum in: Nat Genet 2009, 41: 504.
Arai H, Miyamoto K, Taketani Y, Yamamoto H, Iemori Y, Morita K, et al. A vitamin D receptor gene polymorphism in the translation initiation codon: effect on protein activity and relation to bone mineral density in Japanese women. J Bone Miner Res 1997, 12: 915–921.
Jurutka PW, Remus LS, Whitfield GK, Thompson PD, Hsieh JC, Zitzer H, et al. The polymorphic N terminus in human vitamin D receptor isoforms influences transcriptional activity by modulating interaction with transcription factor IIB. Mol Endocrinol 2000, 14: 401–420.
Shen L, Jia J. An overview of genome-wide association studies in Alzheimer’s disease. Neurosci Bull 2016, 32: 183–190.
Berridge MJ. Vitamin D cell signalling in health and disease. Biochem Biophys Res Commun 2015, 460: 53–71.
Burne TH, McGrath JJ, Eyles DW, Mackay-Sim A. Behavioural characterization of vitamin D receptor knockout mice. Behav Brain Res 2005, 157: 299–308.
Basit S. Vitamin D in health and disease: a literature review. Br J Biomed Sci 2013, 70: 161–172.
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Sazci, A., Uren, N., Idrisoglu, H.A. et al. The rs2228570 Variant of the Vitamin D Receptor Gene is Associated with Essential Tremor. Neurosci. Bull. 35, 362–364 (2019). https://doi.org/10.1007/s12264-018-0287-6
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DOI: https://doi.org/10.1007/s12264-018-0287-6