encyclopedia of medical concepts
ψ 

beta-Hexosaminidase alpha Chain

More information in Books or onNLM PubMed
Definition: The alpha subunit of hexosaminidase A. Mutations in the gene that encodes this protein can result in loss of hexosaminidase A activity and are linked to TAY-SACHS DISEASE.      Other names beta N Acetylhexosaminidase alpha Chain; beta Hexosaminidase alpha Chain; alpha Chain, beta-N-Acetylhexosaminidase; alpha Chain, beta-Hexosaminidase; beta-N-Acetylhexosaminidase alpha Chain; Hexosaminidase A, alpha Chain
 
SubstanceCAS Registry & nameCategoriesSourceDrugs*
HEXA protein, human  EC 3.2.1.52   *beta-Hexosaminidase alpha Chain Tay-Sachs Disease.

To share this definition, click "text" (Facebook, Twitter) or "link" (blog, mail) then paste text link
Ads by Google

Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

Warning: the drugs or drug combinations referred to here may be similar or related, but are not be the same ones and may not have the same pharmacological action as other substances described on the same page or in the same row. Please refer to product monograph or to your doctor
This website is accredited by Health On the Net Foundation. Click to verify.
We comply with the HONcode standard for trustworthy health information: verify here.
About Reference.MD Privacy