MeCP2 Deficiency Leads to Loss of Glial Kir4.1

Rett syndrome (RTT) is an X-linked neurodevelopmental disorder usually caused by mutations in methyl-CpG-binding protein 2 (MeCP2). RTT is typified by apparently normal development until 6–18 mo of age, when motor and communicative skills regress and hand stereotypies, autonomic symptoms, and seizur...

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Bibliografiset tiedot
Julkaisussa:eNeuro
Päätekijät: Kahanovitch, Uri, Cuddapah, Vishnu A., Pacheco, Natasha L., Holt, Leanne M., Mulkey, Daniel K., Percy, Alan K., Olsen, Michelle L.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Society for Neuroscience 2018
Aiheet:
New Research
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5818552/
https://ncbi.nlm.nih.gov/pubmed/29464197
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/ENEURO.0194-17.2018
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