Research of Usher Syndrome, Type I has been linked to Usher Syndrome, Retinitis Pigmentosa, Complete Hearing Loss, Sensorineural Hearing Loss (disorder), Deafness Congenital. The study of Usher Syndrome, Type I has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Usher Syndrome, Type I include Swimming, Mrna Splicing, Translation, Cell Development, Cell Growth. These pathways complement our catalog of research reagents for the study of Usher Syndrome, Type I including antibodies and ELISA kits against MYO7A, USH1C, CDH23, PCDH15, USH1G.
Usher Syndrome, Type I 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 Usher Syndrome, Type I below!
For more information on how to use Laverne, please read the How to Guide.
We have 271 products for the study of Usher Syndrome, Type I that can be applied to Flow Cytometry, Western Blot, Chromatin Immunoprecipitation, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.