Myf-6 Polyclonal Antibody, 100ul Vessels Defects in this gene are

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

HOXA6 is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression

phorbol ester and inflammatory cytokine TNF and IL-1

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Myf-6 Polyclonal Antibody, 100ul Vessels Defects in this gene areMyogenic 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