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TGM6 might not be a specific causative gene for spinocerebellar ataxia resulting from genetic analysis and functional study. Gene 2021 Feb 145495. Cheng Hao-Ling, Dong Hai-Lin, Liu De-Shan, Ni Wang, Ma Yin, Yang Lu, Du Yi-Chu, Chen Dian-Fu, Dong Yi, Wu Zhi-Yi |
A significant inflation in TGM6 genetic risk casts doubt in its causation in spinocerebellar ataxia type 35. Parkinsonism & related disorders 2019 1 63 42-45. Fung Jasmine L F, Tsang Mandy H Y, Leung Gordon K C, Yeung Kit San, Mak Christopher C Y, Fung Cheuk Wing, Chan Sophelia H S, Yu Mullin H C, Chung Brian H |
Genetic Variants Associated with Episodic Ataxia in Korea. Scientific reports 2017 10 7 (1): 13855. Choi Kwang-Dong, Kim Ji-Soo, Kim Hyo-Jung, Jung Ileok, Jeong Seong-Hae, Lee Seung-Han, Kim Dong Uk, Kim Sang-Ho, Choi Seo Young, Shin Jin-Hong, Kim Dae-Seong, Park Kyung-Pil, Kim Hyang-Sook, Choi Jae-Hw |
Mutations in rare ataxia genes are uncommon causes of sporadic cerebellar ataxia. Movement disorders : official journal of the Movement Disorder Society 2012 Mar 27 (3): 442-6. Fogel Brent L, Lee Ji Yong, Lane Jessica, Wahnich Amanda, Chan Sandy, Huang Alden, Osborn Greg E, Klein Eric, Mamah Catherine, Perlman Susan, Geschwind Daniel H, Coppola Giovan |
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