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Research Article

Spinocerebellar Ataxia Type 28 (SCA28) is an Uncommon Cause of Dominant Ataxia Among Chinese Kindreds

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Pages 560-562 | Received 25 Feb 2012, Published online: 22 Jun 2012

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Lan Peng, Chunrong Wang, Zhao Chen, Jun-Ling Wang, Bei-Sha Tang & Hong Jiang. (2013) Spinocerebellar Ataxia Type 13 is an Uncommon SCA Subtype in the Chinese Han Population. International Journal of Neuroscience 123:7, pages 450-453.
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Articles from other publishers (5)

Ranita Ghosh Dastidar, Saradindu Banerjee, Piyush Behari Lal & Somasish Ghosh Dastidar. (2023) Multifaceted Roles of AFG3L2, a Mitochondrial ATPase in Relation to Neurological Disorders. Molecular Neurobiology.
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Guohong Tian & Xinghuai Sun. 2022. Neuro-Ophthalmology. Neuro-Ophthalmology 195 225 .
Han-Lin Chiang, Jong-Ling Fuh, Yu-Shuen Tsai, Bing-Wen Soong, Yi-Chu Liao & Yi-Chung Lee. (2021) Expanding the phenotype of AFG3L2 mutations: Late-onset autosomal recessive spinocerebellar ataxia. Journal of the Neurological Sciences 428, pages 117600.
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Erin Sandford & Margit Burmeister. (2014) Genes and Genetic Testing in Hereditary Ataxias. Genes 5:3, pages 586-603.
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Yu-Tao Liu, Bei-Sha Tang, Jun-Ling Wang, Wen-Juan Guan, Lu Shen, Yu-Ting Shi, Ying Zhou, Xin-Xiang Yan, Kun Xia & Hong Jiang. (2012) Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han population. Neuroscience Letters 528:1, pages 51-54.
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