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A single episode of early-life status epilepticus impacts neonatal ultrasonic vocalization behavior in the Fmr1 knockout mouse
Fragile X Syndrome (FXS) is a genetic disorder caused by a trinucleotide (CGG) expansion mutation in the Fmr1 gene located on the X chromosome. FXS is characterized by hyperactivity, increased anxiety, repetitive-stereotyped behaviors, and impaired language development. Many children diagnosed with...
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| Vydáno v: | Epilepsy Behav |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7541794/ https://ncbi.nlm.nih.gov/pubmed/32693376 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yebeh.2020.107279 |
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