Molecular Basis of Rett Syndrome and Related Disorders (Q167320): Difference between revisions

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Rett Syndrome
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Fragile X Syndrome
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MeCP2
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Neurological Disease
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Synaptic Function
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Autism
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mGluR theory
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Dendritic Spines
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Brain Development
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Genetic Mutations

Latest revision as of 21:08, 12 September 2024

Study of genetic mutations & brain development behind Rett syndrome & related conditions.
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.

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