Genetic analysis of the CHCHD2 gene in a cohort of Chinese patients with Parkinson disease

•CHCHD2 mutations may be rare in Chinese ADPD patients.•The result will stimulate researches about pathogenic role of the CHCHD2 gene.•The association of CHCHD2 mutations in PD needs to be assessed in more samples and other studies. CHCHD2 has been recently reported as a causative gene for autosomal...

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Veröffentlicht in:Neuroscience letters 2016-08, Vol.629, p.116-118
Hauptverfasser: Wu, Hongwei, Lu, Xingjiao, Xie, Fei, Cen, Zhidong, Zheng, Xiaosheng, Luo, Wei
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Sprache:eng
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