Published 2001
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Glut-1 Deficiency Syndrome and Familial Epilepsy
- Creators
- Millichap, J. Gordon
Abstract
A family with autosomal dominant Glut-1 deficiency syndrome (DS) affecting 5 members over 3 generations is reported from the University of Goettingen, Germany; and Columbia University, New York.
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PNB-15-74.pdf
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Additional details
- Other
- PNB-15-74
- Created
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2001When the item was originally created.