N‐Acetylaspartic aciduria: report of three new cases in children with a neurological syndrome associating macrocephaly and leukodystrophy
- 1 September 1988
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 11 (3) , 307-308
- https://doi.org/10.1007/bf01800378
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- 3‐Methylglutaconic aciduria: Familial neonatal form with fatal onsetJournal of Inherited Metabolic Disease, 1987
- 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