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Fragile X Mental Retardation Protein Restricts Small Dye Iontophoresis Entry into Central Neurons
Fragile X mental retardation protein (FMRP) loss causes Fragile X syndrome (FXS), a major disorder characterized by autism, intellectual disability, hyperactivity, and seizures. FMRP is both an RNA- and channel-binding regulator, with critical roles in neural circuit formation and function. However,...
Shranjeno v:
| izdano v: | J Neurosci |
|---|---|
| Main Authors: | , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Society for Neuroscience
2017
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5637114/ https://ncbi.nlm.nih.gov/pubmed/28887386 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.0723-17.2017 |
| Oznake: |
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