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Human placental beta-galactosidase. Characterization of the dimer and complex forms of the enzyme.

GM1 ganglioside beta-galactosidase (beta-Gal) is deficient in the autosomal recessive disorder GM1 gangliosidosis. A portion of the enzyme occurs in a complex with neuraminidase and an additional glycoprotein, protective protein, but the nature of the interactions conferring the stability of the com...

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Bibliografski detalji
Glavni autori: Hubbes, M, D'Agrosa, R M, Callahan, J W
Format: Artigo
Jezik:Inglês
Izdano: 1992
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1132870/
https://ncbi.nlm.nih.gov/pubmed/1497620
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