| Individual ID |
00001760 |
| Associated disease |
SBCADD |
| Inheritance |
Familial |
| Diagnosis/Initial |
- |
| Age/Examination |
- |
| Diagnosis/Definite |
- |
| Age/Onset |
00y05m |
| Phenotype/Onset |
- |
| Phenotype details |
clinical presentation; seizures (which stopped), speech development was significantly delayed, mental retardation |
| Protein |
- |
| Age/Diagnosis |
04y |
| Owner name |
Division of Human Genetics, Innsbruck |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Division of Human Genetics, Innsbruck |
| Date created |
2013-04-05 11:51:07 +02:00 (CEST) |
| Date last edited |
2013-05-13 09:38:49 +02:00 (CEST) |