Associated Papers
TGM6 might not be a specific causative gene for spinocerebellar ataxia resulting from genetic analysis and functional study.
Cheng HL et al.
Gene, 2021
A case report of late-onset cerebellar ataxia associated with a rare p.R342W TGM6 (SCA35) mutation.
Manini A et al.
Bmc Neurology, 2020
TGM6 gene mutations in undiagnosed cerebellar ataxia patients.
Yang ZH et al.
Parkinsonism & Related Disorders, 2018
Genetic Variants Associated with Episodic Ataxia in Korea.
Choi KD et al.
Scientific Reports, 2017
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