Striatin Polyclonal Antibody, 20ul High Speed Micro-Centrifuges Defects in this gene are

Defects in this gene are a cause of mitochondrial pyruvate carrier deficiency

by hydroxylation of the side chain

DCX encodes a member of the doublecortin family

CYP7B1 (cytochrome P450 family 7 subfamily B member 1) encodes a member of the cytochrome P450 superfamily of enzymes

Carbonic anhydrases (CAs) are members of a large family of zinc metalloenzymes responsible for catalyzing the reversible hydration of carbon dioxide

Striatin Polyclonal Antibody, 20ul High Speed Micro-Centrifuges Defects in this gene areCalmodulin binding protein which may function as scaffolding or signaling protein and may play a role in dendritic Ca(2+) signaling.