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Bruck Syndrome 1: Disease Bioinformatics
Research of Bruck Syndrome 1 has been linked to Osteogenesis Imperfecta, Muscle Contracture, Fracture, Arthropathy, Dentinogenesis Imperfecta. The study of Bruck Syndrome 1 has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Bruck Syndrome 1 include Dentinogenesis, Pathogenesis. These pathways help researchers to better understand Bruck Syndrome 1.
Bruck Syndrome 1 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 Bruck Syndrome 1 below!
For more information on how to use Laverne, please read the How to Guide
Top Research Reagents
Bruck Syndrome 1 has been linked to:
Bruck Syndrome 1 has been studied in relation to diseases such as:
Bruck Syndrome 1 has been studied in relation to posttranslational modifications (PTMs) including:
Alternate NamesBruck Syndrome 1 is also known as bruck syndrome 1, osteogenesis imperfecta with congenital joint contractures, brks1.