SVIP Rabbit Polyclonal Antibody, 50ul PCR Series Mutations in SLC52A2 have been

Mutations in SLC52A2 have been associated with Brown-Vialetto-Van Laere syndrome 2--an autosomal recessive progressive neurologic disorder characterized by deafness

This gene encodes a tumor suppressor that is involved in transcriptional and post-transcriptional control pathways

cAMP and cGMP function as key regulators of many important physiological processes

a severe intrahepatic cholestasis that results in transient neonatal jaundice

The protein phosphorylates several target proteins and has a role in neutral amino acid transport and activation of potassium and chloride channels

SVIP Rabbit Polyclonal Antibody, 50ul PCR Series Mutations in SLC52A2 have been