GATM Rabbit Polyclonal Antibody, 100ul Hepatocytes Defects in this gene are

Defects in this gene are a cause of xeroderma pigmentosum complementation group F (XP-F)

Diseases associated with HSPA14 include tetralogy of fallot

both of which contain a SH3 domain and the immunoreceptor tyrosine-based activation motif (ITAM)

coli mismatch repair gene mutS

GATM Rabbit Polyclonal Antibody, 100ul Hepatocytes Defects in this gene areThis gene encodes a mitochondrial enzyme that belongs to the amidinotransferase family. This enzyme is involved in creatine biosynthesis whereby it catalyzes the transfer of a guanido group from L arginine to glycine resulting in guanidinoacetic acid the immediate precursor of creatine. Mutations in this gene cause arginine: glycine amidinotransferase deficiency an inborn error of creatine synthesis characterized by mental retardation language