Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 4.1.1.37 extracted from

  • Aarsand, A.K.; Boman, H.; Sandberg, S.
    Familial and sporadic porphyria cutanea tarda: characterization and diagnostic strategies (2009), Clin. Chem., 55, 795-803.
    View publication on PubMed

Application

Application Comment Organism
diagnostics uroporphyrinogen decarboxylase activity has a high diagnostic accuracy for differentiating the 2 Porphyria cutanea tarda types, the sporadic (sPCT) and familial (fPCT) forms, which are generally clinically indistinguishable, a model that takes into account both clinical information and laboratory test results can be used to predict fPCT Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
erythrocyte
-
Homo sapiens
-

Synonyms

Synonyms Comment Organism
UroD
-
Homo sapiens
uroporphyrinogen decarboxylase
-
Homo sapiens