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) gene leading to the absence of the encoded fragile X mental retardation protein 1 (FMRP). We describe morphological and behavioral abnormalities for both affected hum...
| Publié dans: | Neural plasticity. - 1998. - 8(2001), 4 vom: 03., Seite 285-98 |
|---|---|
| Auteur principal: | |
| Autres auteurs: | |
| Format: | Article |
| Langue: | English |
| Publié: |
2001
|
| Accès à la collection: | Neural plasticity |
| Sujets: | Journal Article Research Support, Non-U.S. Gov't Amino Acids Fmr1 protein, mouse Nerve Tissue Proteins RNA-Binding Proteins Glutamine 0RH81L854J 3,4-Dihydroxyphenylacetic Acid 102-32-9 plus... |