Characterization of a mutation in a family with saposin B deficiency: a glycosylation site defect.

Saposins are small, heat-stable glycoproteins required for the hydrolysis of sphingolipids by specific lysosomal hydrolases. Saposins A, B, C, and D are derived by proteolytic processing from a single precursor protein named prosaposin. Saposin B, previously known as SAP-1 and sulfatide activator, s...

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Dades bibliogràfiques

Publicat a:	Proc Natl Acad Sci U S A
Autors principals:	Kretz, K A, Carson, G S, Morimoto, S, Kishimoto, Y, Fluharty, A L, O'Brien, J S
Format:	Artigo
Idioma:	Inglês
Publicat:	National Academy of Sciences 1990
Matèries:	Research Article
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC53725/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2320574/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.87.7.2541
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