Title : High prevalence of and potential mechanisms for chronic kidney disease in patients with acute intermittent porphyria.

Pub. Date : 2015 Aug

PMID : 25830761






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Acute intermittent porphyria (AIP) is a genetic disorder of the synthesis of heme caused by a deficiency in hydroxymethylbilane synthase (HMBS), leading to the overproduction of the porphyrin precursors delta-aminolevulinic acid and porphobilinogen. Porphyrins hydroxymethylbilane synthase Homo sapiens
2 Acute intermittent porphyria (AIP) is a genetic disorder of the synthesis of heme caused by a deficiency in hydroxymethylbilane synthase (HMBS), leading to the overproduction of the porphyrin precursors delta-aminolevulinic acid and porphobilinogen. Porphyrins hydroxymethylbilane synthase Homo sapiens