Myf-6 Polyclonal Antibody, 50ul Reservoirs the oxytocin receptor

the oxytocin receptor

Mutations in this gene lead to several diseases: Emery-Dreifuss muscular dystrophy

whose genes encode calcium dependent cell-cell adhesion glycoproteins

PTPRN2 (protein tyrosine phosphatase

Multiple alternatively spliced transcript variants encoding the same isoform have been found for FGFRL1

Myf-6 Polyclonal Antibody, 50ul Reservoirs the oxytocin receptorMyogenic factor 6 encoded by MYF6 is a probable basic helix loop helix (bHLH) DNA binding protein involved in muscle differentiation. The encoded protein likely acts as a heterodimer with another bHLH protein. Defects in this gene are a cause of autosomal dominant centronuclear myopathy (ADCNM). Diseases associated with MYF6 include myopathy, centronuclear, 3 and myopathy, centronuclear. Among its related pathways are Developmental Biology and CDO in