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This review of the evidence indicating whether UA may have a protective role in the development and/or progression of PD draws on the findings of reduced serum UA in PD, critically assesses the more equivocal genetic results, and discusses experimental observations that UA may provide protection against the pathogenic mechanisms of PD
Growth retardation and skeletal abnormalities arise from disrupted nucleic acid metabolism and impaired osteoblast activity [5, 6]
Proper dosing and a gradual increase help minimize these effects.
A., Smith, C
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