## Abstract GM1 gangliosidosis is due to ฮฒโgalactosidase deficiency. Only patients with type 3 disease survive into adulthood and develop movement disorders. Clinical descriptions of this form are rare, particularly in nonโJapanese patients. We describe four new patients and systematically analyze
โฆ LIBER โฆ
Parkinsonism in adult-onset GM2 gangliosidosis
โ Scribed by R. Inzelberg; A. D. Korczyn
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 639 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0885-3185
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