Research of Succinate-semialdehyde Dehydrogenase Deficiency has been linked to Inborn Errors Of Metabolism, Muscle Hypotonia, Epilepsy, Ataxia, Developmental Delay (disorder). The study of Succinate-semialdehyde Dehydrogenase Deficiency has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Succinate-semialdehyde Dehydrogenase Deficiency include Pathogenesis, Excretion, Transport, Urea Cycle, Tricarboxylic Acid Cycle. These pathways complement our catalog of research reagents for the study of Succinate-semialdehyde Dehydrogenase Deficiency including antibodies and ELISA kits against ALDH5A1, SUCCINIC SEMIALDEHYDE DEHYDROGENASE, ABAT, LAMC2, CSF2.
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Succinate-semialdehyde Dehydrogenase Deficiency below!
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We have 1637 products for the study of Succinate-semialdehyde Dehydrogenase Deficiency that can be applied to Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Western Blot from our catalog of antibodies and ELISA kits.
Succinate-semialdehyde Dehydrogenase Deficiency is also known as 4-hydroxybutyric Aciduria, Gabauria, Gamma-hydroxybutyric Aciduria, Ssadh Deficiency, Succinic Semialdehyde Dehydrogenase Deficiency.