SL9A3 Polyclonal Antibody, 20ul Cell Culture & Maintenance Mutations in this gene cause

Mutations in this gene cause Joubert syndrome

Mutations in this gene may underlie hereditary disorders of balance and hearing

Each beta4GalT member has a distinct function in the biosynthesis of different glycoconjugates and saccharide structures

with identical protein backbones but different glycosylation profiles

SL9A3 Polyclonal Antibody, 20ul Cell Culture & Maintenance Mutations in this gene causeThe protein encoded by this gene is an epithelial brush border Na H exchanger that uses an inward sodium ion gradient to expel acids from the cell. Defects in this gene are a cause of congenital secretory sodium diarrhea. Pseudogenes of this gene exist on chromosomes 10 and 22.