Prenatal detection of Canavan disease
- 23 March 1991
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 337 (8743) , 735-736
- https://doi.org/10.1016/0140-6736(91)90323-h
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- 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