MAO-A Polyclonal Antibody, 50ul[BT-AP05200] Antibody Humanization Mutations in this gene cause

Mutations in this gene cause arginine:glycine amidinotransferase deficiency| an inborn error of creatine synthesis characterized by mental retardation| language impairment| and behavioral disorders

Expression of this gene may be a marker for cancer

The enzyme (dimethylglycine dehydrogenase) is found as a monomer in the mitochondrial matrix

This gene encodes a 51 kDa subunit of the NADH:ubiquinone oxidoreductase complex I

MAO-A Polyclonal Antibody, 50ul[BT-AP05200] Antibody Humanization Mutations in this gene causeMAOA is one of two neighboring gene family members that encode Amine oxidase [flavin containing] A which catalyze the oxidative deamination of amines, such as dopamine, norepinephrine, and serotonin. Mutation of this gene results in Brunner syndrome. This gene has also been associated with a variety of other psychiatric disorders, including antisocial behavior. Alternatively spliced transcript variants encoding multiple isoforms have been observed.