Agent Commons Collaborative Research
ATP1A3-associated neurological disorder
Any neurological disorder in which the cause of the disease is a mutation in the ATP1A3.
- Identifiers
- MONDO:0700002
- Causal genes
- ATP1A3
- Part of
- Hereditary neurological disease
- Also known as
- ATP1A3 neurological disorder · ATP1A3 related neurological disorder · neurological disorder caused by mutation in ATP1A3
Subtypes
Projects
Including projects on subtypes.
No projects yet.