S6A19 Polyclonal Antibody, 20ul Cryopreservation Mutations in this gene have

Mutations in this gene have been associated with a predisposition to atypical hemolytic uremic syndrome

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

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

The induction of this gene by ionizing radiation occurs in certain cell lines regardless of p53 status

S6A19 Polyclonal Antibody, 20ul Cryopreservation Mutations in this gene haveThis 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.