Known Diseases associated with this Protein: | DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND
| EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16
| EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 16 (EIEE16)
| FAMILIAL INFANTILE MYOCLONIC EPILEPSY (FIME)
| MYOCLONIC EPILEPSY, INFANTILE, FAMILIAL
| SEIZURES SYNDROME
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|  | Tips:  The Domains on the Default View are decided by the Domain's E-Value.  Clicking a check box will display or hide the correlated domain.  To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic. |
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