Title : Evidence for neurological dysfunction in end-stage protoporphyric liver disease.

Pub. Date : 1993 Dec

PMID : 8244265






1 Functional Relationships(s)
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1 Protoporphyria is a genetic disorder characterized by a defect in the enzyme ferrochelatase, which catalyzes the chelation of iron to protoporphyrin. Iron ferrochelatase Homo sapiens