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GM1 gangliosidosis
A rare lysosomal storage disorder characterized biochemically by deficient beta-galactosidase activity and clinically by a wide range of variable neurovisceral, ophthalmological and dysmorphic features.
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GM1 gangliosidosis type 1 3 trials
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GM1 gangliosidosis type 2 3 trials
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GM1 gangliosidosis type 3 0 trials