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- W4242204677 abstract "GM2 gangliosidosis is due to β-hexosaminidase deficiency. Movement disorders can be observed in late-onset forms, and may include tremor, dystonia, parkinsonism, chorea, athetosis, and tremor. Other neurological and psychiatric features are usually present. Diagnosis is based on β-hexosaminidase assay and molecular analysis." @default.
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- W4242204677 date "2010-01-01" @default.
- W4242204677 modified "2023-10-17" @default.
- W4242204677 title "GM2 Gangliosidosis" @default.
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- W4242204677 doi "https://doi.org/10.1016/b978-0-12-374105-9.00330-0" @default.
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