Cell line GM-4390 deficient in lysosomalα-galactosidase activity
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Clinical Biochemistry,Developmental Biology,Cell Biology,Developmental Biology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/BF02630903.pdf
Reference11 articles.
1. Cooper, J. E. K. Microtest plates. A. Single cell clones. In: Kruses, P. F., Jr.; Patterson, M. K., Jr., eds. Tissue culture methods and applications. New York: Academic Press; 1973:266–269.
2. Dawson, G.; Sweeley, C.; Matalon, R., et al. Chemical abnormalities of cultured fibroblasts in Fabry’s disease. Fed. Proc. 28(2):540; 1969.
3. Furbish, F. S.; Blair, H. E.; Shiloach, J., et al.. Enzyme replacement therapy in Gaucher’s disease: Large-scale purification of glucocerebrosidase suitable for human administration. Proc. Natl. Acad. Sci. USA 74(8):3560–3563; 1977.
4. Gal, A. E.; Brady, R. O.; Hibbert, S. R., et al. A practical chromogenic procedure for the determination of homozygotes and heterozygous carriers of Niemann-Pick disease. New Eng. J. of Med. 292(13):632–636; 1975.
5. Kint, J. A. Fabry’s disease: Alpha-galactosidase deficiency. Science 167:1268–1269; 1970.
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