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An autosomal recessive form of hereditary axonal motor neuropathy associated with neuromyotonia has been linked to loss-of-function mutations of HINT1, which encodes histidine triad nucleotide-binding protein 1, a type of purine phosphoramidase

Consult your physician if you have Lebers optic neuropathy, polycythemia, gout, iron or folic acid deficiency anemia or hypokalemia

Pregnant women are advised to ensure adequate folate intake to promote neural tube development, which occurs in the early stages of pregnancy

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LPS-free indicates that the AOD9604 peptide has been manufactured to minimize lipopolysaccharide contamination, which can otherwise interfere with metabolic or inflammatory research data