Huntingtons disease is a neurodegenerative disorder that causes a loss of muscle coordination, cognitive decline and emotional disturbances. The disease is inherited and caused by a mutation of the HTT gene. Huntington’s disease can affect both men and women and symptoms such as involuntary movements, depression, and lack of awareness generally begin to show in patients in their 40s or 50s. Medications are available to manage the symptoms of Huntington Disease; however, there is no known treatment to prevent the physical or mental decline associated with the disease.
Huntington Disease 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 Huntington Disease below!
For more information on how to use Laverne, please read the How to Guide.
We have 1247 products for the study of Huntington Disease that can be applied to Western Blot, Chromatin Immunoprecipitation, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Huntington Disease is also known as Chorea, Huntington's, Chronic Progressive Hereditary Chorea, Huntington Chorea, Huntington's Chorea, Huntington's Disease.
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