The association between UBR1 (Ubiquitin Protein Ligase E3 Component N-Recognin 1) and Muscular Dystrophy is reported, with clinical genetic testing available.
Sources1
Clinical variants0
Symptoms5
Compounds1
Trials0of 2,914 via UBR1 compounds
Publications0
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.