Sialidosis and galactosialidosis: chromosomal assignment of two genes associated with neuraminidase-deficiency disorders.

The inherited human disorders sialidosis and galactosialidosis are the result of deficiencies of glycoprotein-specific alpha-neuraminidase (acylneuraminyl hydrolase, EC 3.2.1.18; sialidase) activity. Two genes were determined to be necessary for expression of neuraminidase by using human-mouse somat...

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Veröffentlicht in:	Proc Natl Acad Sci U S A
Hauptverfasser:	Mueller, O T, Henry, W M, Haley, L L, Byers, M G, Eddy, R L, Shows, T B
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	National Academy of Sciences 1986
Schlagworte:	Research Article
Online-Zugang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC323175/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3081902/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.83.6.1817
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