Hexosaminidase A deficiency presenting as juvenile progressive dystonia.
Open Access
- 1 March 1988
- journal article
- research article
- Published by BMJ in Journal of Neurology, Neurosurgery & Psychiatry
- Vol. 51 (3) , 446-447
- https://doi.org/10.1136/jnnp.51.3.446
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
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- Juvenile spinal muscular atrophy: A new hexosaminidase deficiency phenotypeAnnals of Neurology, 1982
- The clinical spectrum of hexosaminidase deficiency diseasesNeurology, 1981
- A new juvenile hexosaminidase deficiency disease presenting as cerebellar ataxiaNeurology, 1977
- Chronic hexosaminidase A and B deficiencyAnnals of Neurology, 1977
- Late onset GM2-gangliosidosis: Clinical, pathological, and biochemical studies on 8 patientsArchives of Disease in Childhood, 1973
- Juvenile G M2 ‐gangliosidosisNeurology, 1970