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. 2022 Jan;28(1):175-177.
doi: 10.1111/cns.13745. Epub 2021 Oct 21.

Association analysis of SYT11, FGF20, GCH1 rare variants in Parkinson's disease

Affiliations

Association analysis of SYT11, FGF20, GCH1 rare variants in Parkinson's disease

Jia-Li Pu et al. CNS Neurosci Ther. 2022 Jan.
No abstract available

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

FIGURE 1
FIGURE 1
Schematic of human GCH1 and pathogenetic analysis of c.C552T, p.R186C variant. (A) The c.C552T, p.R186C variant locates in GCH1 gene and GCH1 protein. (B) The position and the surrounding sequence of GCH1 p.R186C are highly conserved across different species. (C) Pathogenicity prediction of c.C552T, p.R186C variant in silico. Threshold values for deleteriousness: CADD greater than 15; Polyphen2 greater than 0.86; SIFT less than 0.05 [Colour figure can be viewed at wileyonlinelibrary.com]

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