eEF1A2 binding protein Polyclonal Antibody, 20ul Polyclonal Antibodies this gene is disrupted in

this gene is disrupted in patients with CMT1A (Charcot-Marie-Tooth type 1A) duplication and with HNPP (hereditary neuropathy with liability to pressure palsies) deletion

an alpha chain (GP1BA

An important paralog of this gene is NPY1R

Multiple alternatively spliced transcript variants that encode the same protein have been described for this gene

euthyroid hyperthyroxinaemia

eEF1A2 binding protein Polyclonal Antibody, 20ul Polyclonal Antibodies this gene is disrupted inContains 4 fibronectin type III domains.,Contains 5 Ig like (immunoglobulin like) domains.,subunit: Interacts with KY.,tissue specificity: Expressed in skeletal muscle.,