glutathione peroxidase 1b Frontiers RCSB PDB - 1GP1: THE
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doi: 10.1016/j.pnpbp.2024.111018 173 PatlolaSRDonohoeGMcKernanDP
Mutations in the LRRK2 gene, particularly the most common Gly2019Ser mutation, are seen in patients with autosomal-dominant PD and patients with apparently sporadic PD, who are clinically indistinguishable from patients with idiopathic PD [100]
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Kuehn, D., Beinersdorf, F., Simnofske, M., Bernhard, F., & Kirchner, F
