Aspartoacylase Deficiency: The Enzyme Defect in Canavan Disease
- 1 April 1989
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 12 (S2), 329-331
- https://doi.org/10.1007/bf03335413
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- N‐Acetylaspartic aciduria: report of three new cases in children with a neurological syndrome associating macrocephaly and leukodystrophyJournal of Inherited Metabolic Disease, 1988
- Aspartoacylase deficiency and N‐acetylaspartic aciduria in patients with canavan diseaseAmerican Journal of Medical Genetics, 1988
- N‐acetylaspartic aciduria due to aspartoacylase deficiency — a new aetiology of childhood leukodystrophyJournal of Inherited Metabolic Disease, 1986
- N-Acetylaspartic aciduria in a child with a progressive cerebral atrophyClinica Chimica Acta; International Journal of Clinical Chemistry, 1986
- Diagnosis of organic acidemias by gas chromatography--mass spectrometry.1981
- Hurler's syndrome: biosynthesis of acid mucopolysaccharides in tissue culture.Proceedings of the National Academy of Sciences, 1966