Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Ataxia and RAI1[original query] |
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ATXN3, ATXN7, CACNA1A, and RAI1 Genes and Mitochondrial Polymorphism A10398G Did Not Modify Age at Onset in Spinocerebellar Ataxia Type 2 Patients from South America. Cerebellum (London, England) 2015 Apr . Pereira Fernanda S, Monte Thais L, Locks-Coelho Lucas D, Silva Amanda S P, Barsottini Orlando, Pedroso José L, Cornejo-Olivas Mario, Mazzetti Pilar, Godeiro Clecio, Vargas Fernando R, Lima Maria-Angélica F D, van der Linden Hélio, Toralles Maria Betânia Pereira, Medeiros Paula F V, Ribeiro Erlane, Braga-Neto Pedro, Salarini Diego, Castilhos Raphael M, Saraiva-Pereira Maria-Luiza, Jardim Laura Bannach, |
Neurological phenotypes in spinocerebellar ataxia type 2: Role of mitochondrial polymorphism A10398G and other risk factors. Parkinsonism & related disorders 2017 Jun . Monte Thais Lampert, Pereira Fernanda Santos, Reckziegel Estela da Rosa, Augustin Marina Coutinho, Locks-Coelho Lucas Dorídio, Santos Amanda Senna P, Pedroso José Luiz, Barsottini Orlando, Vargas Fernando Regla, Saraiva-Pereira Maria-Luiza, Jardim Laura Bannach, |
(CAG) loci as genetic modifiers of age at onset in patients with spinocerebellar ataxia type 1 from mainland China. European journal of neurology 2019 Mar . Wang P, Chen Z, Peng Y, Cao L, Li X, Wang C, Yang H, Peng H, Shi Y, Zhou X, Li T, Feng L, Wu C, Qiu R, Xia K, Tang B, Jiang |
Effect of CAG repeats on the age at onset of patients with spinocerebellar ataxia type 2 in China. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2021 9 46 (8): 793-799. Li Yu, Liu Zhen, Hou Xiaorong, Chen Zhao, Shen Lu, Xia Kun, Tang Beisha, Jiang Hong, Wang Junli |
Identifying unstable CNG repeat loci in the human genome: a heuristic approach and implications for neurological disorders. Human genome variation 2024 6 11 (1): 25. Varun Suroliya, Bharathram Uppili, Manish Kumar, Vineet Jha, Achal K Srivastava, Mohammed Far |
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