SG3A2 Polyclonal Antibody, 100ul Low-speed Centrifuges Mutations in this gene may

Mutations in this gene may be associated with Parkinson's disease

Alternative splicing or deletion caused by a translocation event in this paternally-expressed region is responsible for Angelman syndrome or Prader-Willi syndrome due to parental imprint switch failure

troponin T

three PHD zinc fingers

This receptor functions as a ligand-gated ion channel

SG3A2 Polyclonal Antibody, 100ul Low-speed Centrifuges Mutations in this gene mayThe protein encoded by this gene is a secreted lung surfactant protein and a downstream target of thyroid transcription factor. A single nucleotide polymorphism in the promoter of this gene results in susceptibility to asthma.