Molecular Basis of Rett Syndrome and Related Disorders (Q167320): Difference between revisions
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Revision as of 12:18, 8 September 2024
Study of genetic mutations & brain development behind Rett syndrome & related conditions.
- Rett Syndrome
- Fragile X Syndrome
- MeCP2
- Neurological Disease
- Synaptic Function
- Autism
- mGluR theory
- Dendritic Spines
- Brain Development
- Genetic Mutations
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Molecular Basis of Rett Syndrome and Related Disorders |
Study of genetic mutations & brain development behind Rett syndrome & related conditions. |
|
