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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Mueller, O T, Henry, W M, Haley, L L, Byers, M G, Eddy, R L, Shows, T B
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1986
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC323175/
https://ncbi.nlm.nih.gov/pubmed/3081902
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