Glut-1 Deficiency Syndrome and Familial Epilepsy
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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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2001-10-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/1708 |