I-Cell disease, mucolipidosis II
- 1 January 1973
- journal article
- research article
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 114 (4), 259-292
- https://doi.org/10.1007/bf00569920
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- A hypothesis for I-cell disease: Defective hydrolases that do not enter lysosomesBiochemical and Biophysical Research Communications, 1972
- Hurler's syndrome, an a-L-iduronidase deficiencyBiochemical and Biophysical Research Communications, 1972
- Clinical, biochemical, and ultrastructural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue cultureThe Journal of Pediatrics, 1971
- I-cell disease: A clinical pictureThe Journal of Pediatrics, 1971
- Generalized gangliosidosisThe Journal of Pediatrics, 1969
- CLINICAL, BIOCHEMICAL AND ULTRASTRUCTURAL STUDIES OF AN ATYPICAL FORM OF MUCOPOLYSACCHARIDOSISActa Paediatrica, 1969
- Mutant Enzymatic and Cytological Phenotypes in Cultured Human FibroblastsScience, 1967
- A NEW MUCOPOLYSACCHARIDE LIPIDSTORAGE DISEASE?The Lancet, 1966
- The remarkable cells cultured from a human with Hurler’s syndrome: An approach to visual selection forin vitro genetic studiesIn Vitro Cellular & Developmental Biology - Plant, 1966
- Membranous Cytoplasmic Granules in Infantile Amaurotic IdiocyNature, 1960