Full text
PDFPage 5P
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Brown B. I., Brown D. H. The experimental production of glycogen storage in cultured human fibroblasts. Biochem Biophys Res Commun. 1972 Feb 16;46(3):1292–1298. doi: 10.1016/s0006-291x(72)80115-3. [DOI] [PubMed] [Google Scholar]
- Dancis J., Hutzler J., Lynfield J., Cox R. P. Absence of acid maltase in glycogenesis type 2(Pompe's disease) in tissue culture. Am J Dis Child. 1969 Jan;117(1):108–111. doi: 10.1001/archpedi.1969.02100030110013. [DOI] [PubMed] [Google Scholar]
- Hsia D. Y. Study of hereditary metabolic diseases using in vitro techniques. Metabolism. 1970 Apr;19(4):309–339. doi: 10.1016/0026-0495(70)90129-0. [DOI] [PubMed] [Google Scholar]
- Lake B. D. The histochemical evaluation of the glycogen storage diseases. A review of techniques and their limitations. Histochem J. 1970 Sep;2(5):441–450. doi: 10.1007/BF01004725. [DOI] [PubMed] [Google Scholar]
- Matalon R., Dorfman A. Acid mucopolysaccharides in cultured human fibroblasts. Lancet. 1969 Oct 18;2(7625):838–841. doi: 10.1016/s0140-6736(69)92289-2. [DOI] [PubMed] [Google Scholar]
- Nitowsky H. M., Grunfeld A. Lysosomal alpha-glucosidase in type II glycogenosis; activity in leukocytes and cell cultures in relation to genotype. J Lab Clin Med. 1967 Mar;69(3):472–484. [PubMed] [Google Scholar]