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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Detaylı Bibliyografya
Yayımlandı:Epilepsy Behav
Asıl Yazarlar: Huebschman, Jessica L., Hodges, Samantha L., Reynolds, Conner D., Nolan, Suzanne O., Lugo, Joaquin N.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2020
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Article
Online Erişim: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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