Research of Porphobilinogen Synthase Deficiency has been linked to Disorders Of Porphyrin Metabolism, Porphyrias, Hepatic, Acute Intermittent Porphyria, Liver Diseases, Hereditary Coproporphyria. The study of Porphobilinogen Synthase Deficiency has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Porphobilinogen Synthase Deficiency include Excretion, Pathogenesis, Transport, Translation, Secretion. These pathways complement our catalog of research reagents for the study of Porphobilinogen Synthase Deficiency including antibodies and ELISA kits against DELTA-AMINOLEVULINATE DEHYDRATASE, ALAD, AMBP, AVP, CAT.
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Porphobilinogen Synthase Deficiency below!
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We have 281 products for the study of Porphobilinogen Synthase Deficiency that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Porphobilinogen Synthase Deficiency is also known as Acute Hepatic Porphyria, Ala Dehydratase Deficiency Porphyria, Alad Deficiency, Deficiency Of Porphobilinogen Synthase, Delta-aminolaevulinic Acid Dehydratase Deficiency.