Problems in the clinical interpretation of arylsulfatase A deficiency
- 1 January 1981
- journal article
- letter
- Published by Wiley in American Journal of Medical Genetics
- Vol. 10 (4), 413-415
- https://doi.org/10.1002/ajmg.1320100416
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Retinal Pigment Epithelial Degeneration Associated with Leukocytic Arylsulfatase a DeficiencyAmerican Journal of Ophthalmology, 1980
- Letter to the Editor: About the Inheritance of the Aryl Sulfatase APediatric Research, 1980
- Biochemical, psychometric, and neuropsychological studies in heterozygotes for various lipidosesHuman Genetics, 1980
- Prenatal Diagnosis of Metachromatic Leukodystrophy in a Family with Pseudo Arylsulfatase A Deficiency by the Cerebroside Sulfate Loading TestPediatric Research, 1980
- Low arylsulphatase A activity in a family without metachromatic leukodystrophyClinical Genetics, 1978
- Cerebroside sulfate hydrolysis by fibroblasts from a parent with metachromatic leukodystrophyThe Journal of Pediatrics, 1978
- Apparent biochemical homozygosity in two obligatory heterozygotes for metachromatic leukodystrophyThe Journal of Pediatrics, 1976