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Thermal activation of hexosaminidase A in a genetic compound with Tay-Sachs disease

✍ Scribed by Y. Ben-Yoseph; M. S. Baylerian; T. Momoi; H. L. Nadler


Publisher
Springer
Year
1983
Tongue
English
Weight
743 KB
Volume
6
Category
Article
ISSN
0141-8955

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## Abstract Enzyme‐replacement treatment for metabolic storage disorders has been widely studied using model cell culture systems. This study determines the long‐term fate of human hexosaminidase A supplied to Tay‐Sachs disease brain and lung cells. Hex A retention studies showed that the incorpora