DHE3 Rabbit Polyclonal Antibody, 100ul DNA Oligo Synthesis Defects in MEF2A could be

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

The orthologous mouse gene is imprinted and shows exclusive expression from the maternal allele

including the hexadecapeptide

At least two variants of a similar processed pseudogene have been found on chromosome 2

and is found in a cluster of five alpha subunit genes on chromosome 2

DHE3 Rabbit Polyclonal Antibody, 100ul DNA Oligo Synthesis Defects in MEF2A could beThis gene encodes glutamate dehydrogenase which is a mitochondrial matrix enzyme that catalyzes the oxidative deamination of glutamate to alpha ketoglutarate and ammonia. This enzyme has an important role in regulating amino acid induced insulin secretion. It is allosterically activated by ADP and inhibited by GTP and ATP. Activating mutations in this gene are a common cause of congenital hyperinsulinism. Alternative splicing of this gene results in