GLUT1 deficiency syndrome is a disorder that mostly affects the brain. People who are affected by GLUT1 deficiency generally have seizures beginning in the first few months of life. Babies with GLUT1 deficiency syndrome typically have a normal sized head when they are born, but as the brain and skull develop the overall rate of growth is often slower than normal. People with GLUT1 deficiency syndrome may have developmental delay or intellectual disability. They may also have other neurological problems, such as stiffness caused by abnormal tensing of the, difficulty with coordination and speech difficulties. This is caused by a mutation in a person’s cells.
Glut-1 Deficiency Syndrome 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 Glut-1 Deficiency Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 579 products for the study of Glut-1 Deficiency Syndrome that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.