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CHCHD2 gene mutations in familial and sporadic Parkinson's disease.
Shi CH, Mao CY, Zhang SY, Yang J, Song B, Wu P, Zuo CT, Liu YT, Ji Y, Yang ZH, Wu J, Zhuang ZP, Xu YM. Shi CH, et al. Neurobiol Aging. 2016 Feb;38:217.e9-217.e13. doi: 10.1016/j.neurobiolaging.2015.10.040. Epub 2015 Nov 6. Neurobiol Aging. 2016. PMID: 26705026
SMPD1 variants in Chinese Han patients with sporadic Parkinson's disease.
Mao CY, Yang J, Wang H, Zhang SY, Yang ZH, Luo HY, Li F, Shi M, Liu YT, Zhuang ZP, Du P, Wang YH, Shi CH, Xu YM. Mao CY, et al. Parkinsonism Relat Disord. 2017 Jan;34:59-61. doi: 10.1016/j.parkreldis.2016.10.014. Epub 2016 Oct 19. Parkinsonism Relat Disord. 2017. PMID: 27814975
TGM6 gene mutations in undiagnosed cerebellar ataxia patients.
Yang ZH, Shi MM, Liu YT, Wang YL, Luo HY, Wang ZL, Shi CH, Xu YM. Yang ZH, et al. Parkinsonism Relat Disord. 2018 Jan;46:84-86. doi: 10.1016/j.parkreldis.2017.07.001. Epub 2017 Jul 4. Parkinsonism Relat Disord. 2018. PMID: 28927799 No abstract available.
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