The goal of this study is to characterize the molecular response of HS patients to brodalumab therapy in skin and serum, and to identify biomarkers of treatment response. Ten participants that receive
Each annotation is identified by its GO term or EC number, as well as its name. The complementary information given includes: the annotation’s average Gini importance over all RF models (‘Average_impo
Glycogen storage disease type V (GSDV, McArdle disease) is a rare genetic myopathy caused by deficiency of the muscle isoform of glycogen phosphorylase (PYGM). This results in a block in the use of mu
