Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Syndrome and SNCA[original query] |
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Variants in the 3'UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expression. European journal of human genetics : EJHG 2012 Dec 20 (12): 1265-9. Schmitt Ina, Wüllner Ullrich, van Rooyen Jan Pierre, Khazneh Hassan, Becker Julian, Volk Alexander, Kubisch Christian, Becker Tim, Kostic Vladimir S, Klein Christine, Ramirez Alfre |
The PD-associated alpha-synuclein promoter Rep1 allele 2 shows diminished frequency in restless legs syndrome. Neurogenetics 2014 Aug 15 (3): 189-92. Lahut Suna, Vadasz David, Depboylu Candan, Ries Vincent, Krenzer Martina, Stiasny-Kolster Karin, Basak A Nazli, Oertel Wolfgang H, Auburger Geo |
Genetic factors influencing frontostriatal dysfunction and the development of dementia in Parkinson's disease. PloS one 2017 12 (4): e0175560. Huertas Ismael, Jesús Silvia, García-Gómez Francisco Javier, Lojo José Antonio, Bernal-Bernal Inmaculada, Bonilla-Toribio Marta, Martín-Rodriguez Juan Francisco, García-Solís David, Gómez-Garre Pilar, Mir Pab |
Genetics of restless legs syndrome: An update. Sleep medicine reviews 2018 06 39 108-121. Jiménez-Jiménez Félix J, Alonso-Navarro Hortensia, García-Martín Elena, Agúndez José A |
SNCA-Rep1 polymorphism correlates with susceptibility and iron deficiency in restless legs syndrome. Parkinsonism & related disorders 2020 Sep 81 12-17. Zhu Xiao-Ying, Wang Hong-Ming, Wu Ting-Ting, Liu Te, Chen Ya-Jing, Li Xuan, Chen Tian-Jiao, Liu Ye, Zhang Xiao-Jin, Wang Xi-Xi, Zhang Yue, Ondo William G, Wu Yun-Che |
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