FABRY DISEASE--MOLECULAR AND MODEL THERAPEUTIC STUDIES

Project Details

Description

The purpose of this study is to use the recently cloned gene for alpha-galactosidase A to study Fabry disease at the molecular level. Efforts will be directed to identify the different disease gene mutations and to use molecular biologic techniques to produce large amounts of the enzyme for evaluation of enzyme replacement therapy.
StatusFinished
Effective start/end date1/10/9130/09/93

Funding

  • National Center for Research Resources

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