Research of Homocystinuria has been linked to Ectopia Lentis, Atherosclerosis, Anemia, Inborn Errors Of Metabolism, Hyperhomocysteinemia. The study of Homocystinuria has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Homocystinuria include Pathogenesis, Excretion, Coagulation, Transsulfuration, Methylation. These pathways complement our catalog of research reagents for the study of Homocystinuria including antibodies and ELISA kits against CBS, MTHFR, MMACHC, MTR, MTRR.
Homocystinuria 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 Homocystinuria below!
For more information on how to use Laverne, please read the How to Guide.
We have 565 products for the study of Homocystinuria that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Homocystinuria is also known as homocystinuria, homocystinuria caused by cystathionine beta-synthase deficiency, cystathionine beta synthase deficiency, homocystinuria, cystathionine beta-synthase deficiency, cystathionine beta-synthase deficiency disease, cystathionine beta-synthase deficiency, cystathionine synthase deficiency, homocystinuria (disorder), cbs deficiency.
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