Chain600: Epilepsy, Progressive Myoclonus
This is a rare disease.
Example use A
Rare disease screening of newborns or adults thinking of having children. Could also be used as part of a comprehensive analysis of a person's genes.
Developer
Dr. Colby
Genetic info
Genes | Genetic variants |
---|---|
CSTB | chr21:45194558,chr21:45194213 |
EPM2A | chr6:145948827,chr6:145948713 |