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Of Men and Mice: Modeling the Fragile X Syndrome
The Fragile X Syndrome (FXS) is one of the most common forms of inherited intellectual disability in all human societies. Caused by the transcriptional silencing of a single gene, the fragile x mental retardation gene FMR1, FXS is characterized by a variety of symptoms, which range from mental disab...
Tallennettuna:
| Julkaisussa: | Front Mol Neurosci |
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| Päätekijä: | |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5862809/ https://ncbi.nlm.nih.gov/pubmed/29599705 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnmol.2018.00041 |
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