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Sphingolipid Metabolism Perturbations in Rett Syndrome
Rett syndrome is a severe neurodevelopmental disorder affecting mostly females and is caused by loss-of-function mutations in the MECP2 gene that encoded the methyl-CpG-binding protein 2. The pathogenetic mechanisms of Rett syndrome are not completely understood and metabolic derangements are emergi...
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| Vydáno v: | Metabolites |
|---|---|
| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
MDPI
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6835521/ https://ncbi.nlm.nih.gov/pubmed/31658741 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/metabo9100221 |
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