Myf-6 Polyclonal Antibody, 100ul Vessels maps to chromosome 6p21

maps to chromosome 6p21

and other ovarian cancer cells

Receptor for neuropeptide Y and peptide YY

Defects in this gene are a cause of progressive external ophthalmoplegia with mitochondrial DNA deletions 1 (PEOA1)

Several transcript variants encoding different isoforms have been found for HARS

Myf-6 Polyclonal Antibody, 100ul Vessels maps to chromosome 6p21Myogenic 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