TBD Polyclonal Antibody, 100ul Purification Mutations in this gene are

Mutations in this gene are associated with the French-Canadian type of Leigh syndrome

and mutations in the gene are the cause of 17beta-hydroxysteroid dehydrogenase type 10 (HSD10) deficiency

and expressed in testis and in a significant fraction of tumors of various histological types

while Group III includes GRM4

and a P0 monomer

TBD Polyclonal Antibody, 100ul Purification Mutations in this gene arealternative products: Experimental confirmation may be lacking for some isoforms,In the elongating spermatid it is associated with the manchette, a specialized microtubule system present during reshaping of the sperm head.,Belongs to the tubulin family.,subcellular location: Associated with centrioles. Both cytoplasmic and nuclear.,