Literature DB >> 6784663

GM1 gangliosidosis: enzymatic variation in a single family.

D F Farrell, M P MacMartin.   

Abstract

Acid beta-galactosidase activity can be separated into multiple molecular forms by isoelectric focusing on cellulose acetate membranes. The residual acid beta-galactosidase in the juvenile form of GM1 gangliosidosis has three bands of enzyme activity with an apparent isoelectric pH (pI) range from 4.9 to 5.2, whereas that in the infantile form has a single band with an apparent pI of 5.2. Separation of residual acid beta-galactosidase into multiple molecular forms by analytical isoelectric focusing demonstrates enzymatic differences that can be correlated with the allelic mutations that affect the GM1 ganglioside beta-galactosidase locus.

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Year:  1981        PMID: 6784663     DOI: 10.1002/ana.410090305

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  2 in total

1.  Unilateral retinitis pigmentosa and cone-rod dystrophy.

Authors:  Donald F Farrell
Journal:  Clin Ophthalmol       Date:  2009-06-02

2.  GM1 gangliosidosis, type 2: ocular clinicopathologic correlation.

Authors:  L J Cairns; W R Green; H S Singer
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1984       Impact factor: 3.117

  2 in total

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