EF-Tu Polyclonal Antibody, 100ul Rotator and sensory organ development

and sensory organ development

peripheral blood lymphocytes and bone marrow

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene

component of the NF-kappa-B p50-p50 complex

due to defective resorption of immature bone

EF-Tu Polyclonal Antibody, 100ul Rotator and sensory organ developmentTUFM (Tu translation elongation factor, mitochondrial) encodes a protein which participates in protein translation in mitochondria. Mutations in TUFM have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17.