Myf-6 Polyclonal Antibody, 100ul Vessels and male pseudohermaphtoditism with Leydig

and male pseudohermaphtoditism with Leydig cell hypoplasia

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Myosin heavy chains are encoded by a multigene family

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

Myf-6 Polyclonal Antibody, 100ul Vessels and male pseudohermaphtoditism with LeydigMyogenic 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