Research of Hallervorden-spatz Syndrome has been linked to Nerve Degeneration, Dystonia Disorders, Globus Hystericus, Neurodegenerative Disorders, Movement Disorders. The study of Hallervorden-spatz Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Hallervorden-spatz Syndrome include Pathogenesis, Pigmentation, Localization, Transport, Myelination. These pathways complement our catalog of research reagents for the study of Hallervorden-spatz Syndrome including antibodies and ELISA kits against NEUROAXONAL DYSTROPHY, ACAT1, CP, FXN, GFER.
Hallervorden-spatz 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 Hallervorden-spatz Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 591 products for the study of Hallervorden-spatz Syndrome that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Hallervorden-spatz Syndrome is also known as hallervorden-spatz syndrome, pantothenate kinase-associated neurodegeneration, pkan, nbia1, neurodegeneration with brain iron accumulation 1, pigmentary pallidal degeneration (disorder), brain iron accumulation type i syndrome, neuroaxonal dystrophy, late infantile, neuroaxonal dystrophy, juvenile-onset, neuroaxonal dystrophies, nerve degeneration, hss.