Prenatal diagnosis of Krabbe disease: Galactosylceramide metabolism in cultured amniotic fluid cells
- 30 November 1982
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 101 (5) , 754-757
- https://doi.org/10.1016/s0022-3476(82)80312-0
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
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- An improved method for the identification of patients and carriers of krabbe's diseaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1974
- In utero diagnosis of globoid cell leukodystrophy (Krabbe's disease)Biochemical and Biophysical Research Communications, 1971
- Krabbe's Globoid Cell Leukodystrophy: Deficiency of Galactocerebrosidase in Serum, Leukocytes, and FibroblastsScience, 1971
- Globoid Cell Leucodystrophy (Krabbe's Disease): Deficiency of Galactocerebroside β-GalactosidaseProceedings of the National Academy of Sciences, 1970