Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Ataxia and NOP56[original query] |
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Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement. American journal of human genetics 2011 Jul 89 (1): 121-30. Kobayashi Hatasu, Abe Koji, Matsuura Tohru, Ikeda Yoshio, Hitomi Toshiaki, Akechi Yuji, Habu Toshiyuki, Liu Wanyang, Okuda Hiroko, Koizumi Ak |
Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China. Clinical genetics 2015 Dec . Zeng Sheng, Zeng Junsheng, He Miao, Zeng Xianfeng, Zhou Yao, Liu Zhen, Xia Kun, Pan Qian, Jiang Hong, Shen Lu, Yan Xinxiang, Tang Beisha, Wang Junli |
Spinocerebellar ataxia type 36 in the Han Chinese. Neurology. Genetics 2016 Jun 2 (3): e68. Lee Yi-Chung, Tsai Pei-Chien, Guo Yuh-Cherng, Hsiao Cheng-Tsung, Liu Guan-Ting, Liao Yi-Chu, Soong Bing-W |
Noncoding repeat expansions for ALS in Japan are associated with the ATXN8OS gene. Neurology. Genetics 2018 8 4 (4): e252. Hirano Makito, Samukawa Makoto, Isono Chiharu, Saigoh Kazumasa, Nakamura Yusaku, Kusunoki Susu |
Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36). Cerebellum (London, England) 2020 4 19 (4): 501-509. Martínez-Regueiro R, Arias M, Cruz R, Quintáns B, Labella-Caballero T, Pardo M, Pardo J, García-Murias M, Carracedo A, Sobrido M-J, Fernández-Prieto |
Repeats expansions in ATXN2, NOP56, NIPA1 and ATXN1 are not associated with ALS in Africans. IBRO neuroscience reports 2021 6 10 130-135. Nel Melissa, Mavundla Thandeka, Gultig Kayleigh, Botha Gerrit, Mulder Nicola, Benatar Michael, Wuu Joanne, Cooley Anne, Myers Jason, Rampersaud Evadnie, Wu Gang, Heckmann Jeannine |
Diagnostic Efficacy of Genetic Studies in a Series of Hereditary Cerebellar Ataxias in Eastern Spain. Neurology. Genetics 2022 12 8 (6): e200038. Baviera-Muñoz Raquel, Carretero-Vilarroig Lidón, Vázquez-Costa Juan Francisco, Morata-Martínez Carlos, Campins-Romeu Marina, Muelas Nuria, Sastre-Bataller Isabel, Martínez-Torres Irene, Pérez-García Julia, Sivera Rafael, Sevilla Teresa, Vilchez Juan J, Jaijo Teresa, Espinós Carmen, Millán Jose M, Bataller Luis, Aller Ele |
Repeat expansions in NOP56 are a cause of spinocerebellar ataxia Type 36 in the British population. Brain communications 2023 10 5 (5): fcad244. Tanya Lam, Clarissa Rocca, Kristina Ibanez, Anupriya Dalmia, Samuel Tallman, Marios Hadjivassiliou, Anke Hensiek, Andrea Nemeth, Stefano Facchini, , Nicholas Wood, Andrea Cortese, Henry Houlden, Arianna Tuc |
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- Page last updated:Mar 25, 2024
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