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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| Main Author: | |
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| Format: | Book |
| Published: |
Pediatric Neurology Briefs Publishers,
2001-10-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |