S6A19 Polyclonal Antibody, 20ul Cryopreservation DMD patients carry mutations which

DMD patients carry mutations which cause premature translation termination (nonsense or frame shift mutations)

a repair-deficient mutant that exhibits hypersensitivity to a number of different DNA-damaging agents

Their protein structures resemble small leucine-rich proteoglycans found in the extracellular matrix

a ubiquitin-like post-translational modifier protein

Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly

S6A19 Polyclonal Antibody, 20ul Cryopreservation DMD patients carry mutations whichThis gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder.