Changes in the Cerebrospinal Fluid and Plasma Lipidome in Patients with Rett Syndrome

Rett syndrome (RTT) is defined as a rare disease caused by mutations of the methyl-CpG binding protein 2 (MECP2). It is one of the most common causes of genetic mental retardation in girls, characterized by normal early psychomotor development, followed by severe neurologic regression. Hitherto, RTT...

Descripción completa

Detalles Bibliográficos
Autores principales: Zandl-Lang, Martina, Züllig, Thomas, Trötzmüller, Martin, Naegelin, Yvonne, Abela, Lucia, Wilken, Bernd, Scholl-Buergi, Sabine, Karall, Daniela, Kappos, Ludwig, Köfeler, Harald, Plecko, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026385/
https://www.ncbi.nlm.nih.gov/pubmed/35448478
http://dx.doi.org/10.3390/metabo12040291

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026385/
https://www.ncbi.nlm.nih.gov/pubmed/35448478
http://dx.doi.org/10.3390/metabo12040291

Ejemplares similares