Title : The mutation mechanism causing juvenile-onset Tay-Sachs disease among Lebanese.

Pub. Date : 1989 May

PMID : 2527097






1 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 The measurement of residual enzyme activity in the fibroblasts of patients which best correlated with the onset of the illness was the ion exchange chromatographic separation of Hex A-associated hydrolysis of the synthetic substrate 4-methylumbelliferyl N-acetyl-beta-D-glucosamine-6-sulfate (4MUGS). 4-methylumbelliferyl n-acetyl-beta-d-glucosamine-6-sulfate hexosaminidase subunit alpha Homo sapiens