GABA Measurement in a Neonatal Fragile X Syndrome Mouse Model Using (1)H-Magnetic Resonance Spectroscopy and Mass Spectrometry

Fragile X syndrome (FXS) is the leading monogenetic cause of autism spectrum disorder and inherited cause of intellectual disability that affects approximately one in 7,000 males and one in 11,000 females. In FXS, the Fmr1 gene is silenced and prevents the expression of the fragile X mental retardat...

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Detalles Bibliográficos
Autores principales: Reyes, Samantha T., Mohajeri, Sanaz, Krasinska, Karolina, Guo, Scarlett G., Gu, Meng, Pisani, Laura, Rosenberg, Jarrett, Spielman, Daniel M., Chin, Frederick T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7775297/
https://www.ncbi.nlm.nih.gov/pubmed/33390902
http://dx.doi.org/10.3389/fnmol.2020.612685

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7775297/
https://www.ncbi.nlm.nih.gov/pubmed/33390902
http://dx.doi.org/10.3389/fnmol.2020.612685

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