Published 2001 | Version v1.0.0
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Glut-1 Deficiency Syndrome and Familial Epilepsy

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

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Created
2001
When the item was originally created.