Research of Masa Syndrome (disorder) has been linked to Hydrocephalus, Tissue Adhesions, Paraplegia, Spastic Paraplegia, X-linked Hydrocephalus Syndrome. The study of Masa Syndrome (disorder) has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Masa Syndrome (disorder) include Cell Adhesion, Brain Development, Receptor-mediated Endocytosis, Cell Migration, Translation. These pathways complement our catalog of research reagents for the study of Masa Syndrome (disorder) including antibodies and ELISA kits against L1 PROTEIN, GLUTATHIONE TRANSFERASE, CONGENITAL HYDROCEPHALUS, ACACA, DNTT.
Masa Syndrome (disorder) 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 Masa Syndrome (disorder) below!
For more information on how to use Laverne, please read the How to Guide.
We have 1339 products for the study of Masa Syndrome (disorder) that can be applied to Flow Cytometry, Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
Masa Syndrome (disorder) is also known as Clasped Thumb And Mental Retardation, Crash Syndrome, Masa (mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome, Mental Retardation, Aphasia, Shuffling Gait, And Adducted Thumbs.