SLC13A5 Deficiency Natural History Study - Remote Only
ENROLLING_BY_INVITATION
Status
Conditions
- Citrate Transporter Deficiency
- Epilepsy
- Rare Diseases
- Movement Disorders
- Genetic Disorder
- SLC13A5 Deficiency
- EIEE25
- Kohlschutter-Tonz Syndrome (non-ROGDI)
- 17p13.1 Deletions Confined to SLC13A5 Gene
- Citrate Transporter Disorder
Sponsor
TESS Research Foundation
Collaborators