HEXA gene mutation; beta-N-acetylhexosaminidase alpha gene mutation

Clinical significance

• HEXA gene mutations are the cause of Tay-Sachs disease

More general terms

• gene mutation testing; gene mutation analysis

Additional terms

• beta N-acetyl hexosaminidase alpha chain (hexosaminidase-A, HEXA)
• beta-N-acetylhexosaminidase A in serum
• HEXA gene deletion;