Canavan disease: findings in four new cases
- 1 March 1991
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 14 (2) , 267-268
- https://doi.org/10.1007/bf01800603
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan diseaseAmerican Journal of Medical Genetics, 1989
- 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