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Generation of induced pluripotent stem cell line (ZZUi0021-A) from a patient with spinocerebellar ataxia type 19.

Stem cell research - 1 May 2021

Liu Fen, Fan Yu, Fan Liyuan, Li Mengjie, Zhang Qimeng, Mao Chengyuan, Wu Jun, Zhang Shuo, Hu Zhengwei, Shi Changhe, Xu Yuming

Abstract excerpt

Spinocerebellar ataxia type 19 (SCA19) is an extremely rare autosomal dominant cerebellar ataxia hereditary that caused by the KCND3 gene mutation. And has a complex pathogenesis. At present, its pathogenesis is still unclear, and there is no effective treatment for SCA19. So, to study its pathogenesis and find effective treatments, we collected the fifibroblasts from a patient with SCA19, then successfully...

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PMID: 34087979
DOI: 10.1016/j.scr.2021.102320

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Generation of induced pluripotent stem cell line (ZZUi0021-A) from a patient with spinocerebellar ataxia type 19.PMID 34087979Read ↗

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