Alterations of Amino Acids and Monoamine Metabolism in Male Fmr1 Knockout Mice: A Putative Animal Model of the Human Fragile X Mental Retardation Syndrome

The Fragile X syndrome, a common form of mental retardation in humans, is caused by silencing the fragile X mental retardation (FMR1) geneleading to the absence of the encoded fragile X mental retardation protein 1 (FMRP). We describe morphological and behavioral abnormalities for both affected huma...

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Detalles Bibliográficos
Autores principales: Gruss, Michael, Braun, Katharina
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2001
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2565378/
https://www.ncbi.nlm.nih.gov/pubmed/12018775
http://dx.doi.org/10.1155/NP.2001.285

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2565378/
https://www.ncbi.nlm.nih.gov/pubmed/12018775
http://dx.doi.org/10.1155/NP.2001.285

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