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[Analysis of SCA3/MJD3 gene mutation and genetic polymorphism in a guangxi family with spinocerebellar ataxia 3].

Yi chuan = Hereditas - 1 Nov 2013

Chang Rong-Ni, Yuan Guang-Zhi, Tan Jian-Qiang, Lai Qing-Niao, Ma Jun, Yang Yi-Jin, Shu Wei, Hou Wei, Yuan Zhi-Gang

Abstract excerpt

Autosomal dominant cerebellar ataxias (ADCAs) comprise a group of genetically heterogeneous neurodegenerative disorders among which spinocerebellar ataxia type 3 (SCA3) represents the most common form of SCAs worldwide. The fragments of SCA3/MJD gene,which is the member of family GXPL1,were amplified by polymerase chain reaction (PCR). The PCR products of SCA3/MJD gene were detected with capillary electrophoresis...

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PMID: 24579313
DOI: 10.3724/sp.j.1005.2013.01300

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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