AGT2 Polyclonal Antibody, 20ul Cell Separation and Collection Defects in MEF2A could be

Defects in MEF2A could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1)

|Belongs to the heparin-binding growth factors family

nephronophthisis

PBC enventually leads to cirrhosis and liver failure

The four members of this family are mitogenic factors for cells of mesenchymal origin and are characterized by a core motif of eight cysteines

AGT2 Polyclonal Antibody, 20ul Cell Separation and Collection Defects in MEF2A could beThe protein encoded by this gene is a class III pyridoxal phosphate dependent mitochondrial aminotransferase. It catalyzes the conversion of glyoxylate to glycine using L alanine as the amino donor. It is an important regulator of methylarginines and is involved in the control of blood pressure in kidney. Polymorphisms in this gene affect methylarginine and beta aminoisobutyrate metabolism, and are associated with carotid atherosclerosis. Alternative