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prdx3 protein, human
(compound)
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A novel biallelic variant further delineates PRDX3-related autosomal recessive cerebellar ataxia.
Expanding PRDX3 disease: broad range of onset age and infratentorial MRI signal changes.
A quantitative proteomic analysis reveals the potential roles of PRDX3 in neurite outgrowth in N2a-A…
Confirmation of PRDX3 c.568G>C as the Genetic Basis of Punctiform and Polychromatic Pre-Descemet Cor…
LncRNA LUADT1 inhibits cell apoptosis in diabetic retinopathy by regulating miR-383/peroxiredoxin 3 …
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