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Hexosaminidase isozyme in type O Gm2 gangliosidosis (Sandhoff-Jatzkewitz disease).

The residual enzyme of the fibroblasts of a child with homozygous type 0 GM2 gangliosidosis (Sandhoff-Jatzkewitz disease) has been found to correspond with a minor fraction of enzyme which can be isolated from normal fibroblasts by repeated chromatography. This enzyme is designated as hexosaminidase...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Beutler, E, Kuhl, W, Comings, D
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 1975
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1762825/
https://ncbi.nlm.nih.gov/pubmed/808963
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