|?|| (C;C) (C;G) (G;G) ||28|
[PMID 18205889] Parkinson's disease The risk alleles for each SNP identified from conditional logistic regression, rs1721100 C, rs1721082 T and rs1799836 A, are consistent with previous reports.
Significant interaction between this FGF20 SNP and a MAOB gene SNP, rs1799836 was also noticed.
] Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease.
[PMID 15967032] Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients.
[PMID 17515805] Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population.
[PMID 18252210] Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein.
[PMID 19133659] FGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expression.
[PMID 22342445] Fibroblast growth factor 20 (FGF20) polymorphism is a risk factor for Parkinson's disease in Chinese population.
[PMID 23938014] Fibroblast growth factor 20 polymorphism in sporadic Parkinson's disease in Northern Han Chinese
[PMID 25030126] Quantitative assessment of the association between fibroblast growth factor 20 rs1721100 C/G polymorphism and the risk of sporadic Parkinson's diseases: a meta-analysis