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Deficit in neuraminidase associated with mucolipidosis II (I-cell disease).

作者信息

Strecker G, Michalski J C, Montreuil J, Farriaux J P

出版信息

Biomedicine. 1976 Sep 30;25(7):238-40.

PMID:990381
Abstract

Using a tritiated sialyloligosaccharide as a substrate, the authors showed that mucolipidosis II is characterized by a lack of neuraminidase activity in leucocytes, while the other acidic hydrolases activities are normal. According to Ashwell, terminal galactose is the required signal for glycoproteins uptake by the cells. Thus, a neuraminidase deficit may explain the increase of sialylated hydrolases activities in the plasma and the non-recognition of these enzymes by cultured fibroblasts.

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