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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...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Front Mol Neurosci
Päätekijä: Dahlhaus, Regina
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Frontiers Media S.A. 2018
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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