dopa decarboxylase inhibitor to reduce side effects.
The polyamines are progressively synthesized by decarboxylation from ornithine by a rate limiting enzyme ornithine decarboxylase (ODC ).
The other is a GAD (Glutamic Acid Decarboxylase) autoantibody test.
HEP results from a defect in uroporphyrinogen decarboxylase activity (step 5), and is caused by defects in the same gene as PCT.
PCT is caused by deficient uroporphyrinogen decarboxylase.
PCT is caused by mutations in the uroporphyrinogen decarboxylase gene (UROD) located at 1p34.
HEP is linked to a deficiency of uroporphyrinogen decarboxylase in both the liver and the bone marrow.
HEP is an autosomal recessive disease caused by mutations in the gene responsible for PCT, the uroporphyrinogen decarboxylase gene (UROD), located at 1p34.
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