GM1 Gangliosidosis Type I
What is Gangliosidosis GM1 Type I? GM1-gangliosidosis type I (generalized familial gangliosidosis, neurovisceral lipidosis, b-galactosidase deficiency) is characterized by an autosomal recessively inherited deficiency of the enzyme GM1-b-galactosadase. The activity of this enzyme in the
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