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COG8 peptide

Create: 03/27/2019
Expired Date:never
Category: Medical testing [Health&Medical&Pharmaceutical]
Message:This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance. https://www.creative-diagnostics.com/COG8-peptide-178867-436.htm
City:Shirley[US] 
Location:
 
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