Research of Hereditary Coproporphyria has been linked to Disorders Of Porphyrin Metabolism, Porphyrias, Hepatic, Acute Intermittent Porphyria, Variegate Porphyria, Porphyria Cutanea Tarda. The study of Hereditary Coproporphyria has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Hereditary Coproporphyria include Excretion, Pathogenesis, Translation, Pigmentation, Secretion. These pathways complement our catalog of research reagents for the study of Hereditary Coproporphyria including antibodies and ELISA kits against CPOX, FECH, PPOX, HMBS, CPO.
Hereditary Coproporphyria Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Hereditary Coproporphyria below!
For more information on how to use Laverne, please read the How to Guide.
We have 410 products for the study of Hereditary Coproporphyria that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunohistochemistry, Immunocytochemistry/Immunofluorescence from our catalog of antibodies and ELISA kits.
Hereditary Coproporphyria is also known as hereditary coproporphyria, coproporphyrinogen oxidase deficiency, hereditary coproporphyria porphyria, cpx deficiency, hcp, hereditary coproporphyria (disorder), porphyria hepatica coproporphyria, coproporphyria, hereditary, porphyria hepatica ii.
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