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This gene encodes an enzyme that degrades heparan sulfate by hydrolysis of terminal N-acetyl-D-glucosamine residues in N-acetyl-alpha-D-glucosaminides. Defects in this gene are the cause of mucopolysaccharidosis type IIIB (MPS-IIIB), also known as Sanfilippo syndrome B. This disease is characterized by the lysosomal accumulation and urinary excretion of heparan sulfate.
Alpha-N-acetylglucosaminidase; alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB); Alpha-N-acetylglucosaminidase 77 kDa form; Alpha-N-acetylglucosaminidase 82 kDa form; alpha-N-acetylglucosaminidase, lysosomal; CMT2V; MPS3B; MPS-IIIB; N-acetyl-alpha-glucosaminidase; N-acetyl-glucosaminidase; N-acetylglucosaminidase, alpha; NAG; NAGLU; RGD1564228; testicular tissue protein Li 18; UFHSD; UFHSD1
100 µL
100 µL
100 µg
100 µL
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