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.
Saved in:
| Main Author: | |
|---|---|
| Format: | Book |
| Published: |
Pediatric Neurology Briefs Publishers,
2001-10-01T00:00:00Z.
|
| Subjects: | |
| Online Access: | Connect to this object online. |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Be the first to leave a comment!