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Glial Dysfunction in MeCP2 Deficiency Models: Implications for Rett Syndrome
Rett syndrome (RTT) is a rare, X-linked neurodevelopmental disorder typically affecting females, resulting in a range of symptoms including autistic features, intellectual impairment, motor deterioration, and autonomic abnormalities. RTT is primarily caused by the genetic mutation of the Mecp2 gene....
Tallennettuna:
| Julkaisussa: | Int J Mol Sci |
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| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
MDPI
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6696322/ https://ncbi.nlm.nih.gov/pubmed/31387202 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms20153813 |
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