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Article

Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han population.

Neuroscience letters - 18 Oct 2012

Liu Yu-Tao, Tang Bei-Sha, Wang Jun-Ling, Guan Wen-Juan, Shen Lu, Shi Yu-Ting, Zhou Ying, Yan Xin-Xiang, Xia Kun, Jiang Hong

Abstract excerpt

The spinocerebellar ataxias (SCAs) are a clinically and genetically heterogeneous group of neurodegenerative diseases. In 2010, four missense mutations in the prodynorphin (PDYN) gene were found in two families and two sporadic cases of SCA type 23 (SCA23) from the Netherlands. In addition, one missense mutation in PDYN was also found in one sporadic SCA23 case in America in 2012. To date, there have been no...

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Identifiers

PMID: 22985506
DOI: 10.1016/j.neulet.2012.08.062

Genes

PDYN

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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