| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/ANA.410090510 |
| P698 | PubMed publication ID | 6791575 |
| P2093 | author name string | K Suzuki | |
| T Kobayashi | |||
| P2860 | cites work | Adult (chronic) GM2 gangliosidosis. Atypical spinocerebellar degeneration in a Jewish sibship | Q39977585 |
| Juvenile GM2-gangliosidosis: Clinical variant of Tay-Sachs disease or a new disease | Q48935022 | ||
| Late infantile systemic lipidosis. Major monosialogangliosidosis. Delineation of two types. | Q51188444 | ||
| P433 | issue | 5 | |
| P304 | page(s) | 476-483 | |
| P577 | publication date | 1981-05-01 | |
| P1433 | published in | Annals of Neurology | Q564414 |
| P1476 | title | Chronic GM1 gangliosidosis presenting as dystonia: II. Biochemical studies | |
| P478 | volume | 9 |
| Q68378906 | A case of chronic GM1 gangliosidosis presenting as dystonia: clinical and biochemical studies |
| Q48426037 | Accumulation of lysosphingolipids in tissues from patients with GM1 and GM2 gangliosidoses |
| Q37429324 | Application of lectin histochemistry and carbohydrate analysis to the characterization of lysosomal storage diseases |
| Q42447986 | GM1 gangliosidosis type 3 with severe jaw-closing impairment |
| Q33621191 | Hemidystonia: a report of 22 patients and a review of the literature |
| Q34364491 | Lysosomal multienzyme complex: biochemistry, genetics, and molecular pathophysiology |
| Q38218040 | Pathogenic role of ganglioside metabolism in neurodegenerative diseases |
| Q46305506 | Uptake and metabolism of radiolabelled GM1-ganglioside in skin fibroblasts from controls and patients with GM1-gangliosidosis |
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