Research of Multiple Carboxylase Deficiency has been linked to Biotinidase Deficiency, Inborn Errors Of Metabolism, Holocarboxylase Synthetase Deficiency, Acidosis, Macular Corneal Dystrophy Type I. The study of Multiple Carboxylase Deficiency has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Multiple Carboxylase Deficiency include Excretion, Gluconeogenesis, Transport, Response To Biotin, Intestinal Absorption. These pathways complement our catalog of research reagents for the study of Multiple Carboxylase Deficiency including antibodies and ELISA kits against ACACA, ACADM, AMPD1, AMY2A, BTD.
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Multiple Carboxylase Deficiency below!
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We have 483 products for the study of Multiple Carboxylase Deficiency that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Immunohistochemistry from our catalog of antibodies and ELISA kits.