IIGP5 Polyclonal Antibody, 100ul Cell Screening and Imaging Evidence indicates that mutations in

Evidence indicates that mutations in this gene are responsible for the primary defects in patients with progressive myoclonic epilepsy (EPM1)

F7 encodes coagulation factor VII which is a vitamin K-dependent factor essential for hemostasis

TBX22 is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain

a familial cardiac and skeletal myopathy (CSM)

APOBEC3A is a member of the cytidine deaminase gene family

IIGP5 Polyclonal Antibody, 100ul Cell Screening and Imaging Evidence indicates that mutations inCatalytic activity: GTP + H(2)O = GDP + phosphate. Belongs to the interferon inducible GTPase family.