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...

Descripción completa

Detalles Bibliográficos
Autores principales: Cappuccio, Gerarda, Donti, Taraka, Pinelli, Michele, Bernardo, Pia, Bravaccio, Carmela, Elsea, Sarah H., Brunetti-Pierri, Nicola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835521/
https://www.ncbi.nlm.nih.gov/pubmed/31658741
http://dx.doi.org/10.3390/metabo9100221

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835521/
https://www.ncbi.nlm.nih.gov/pubmed/31658741
http://dx.doi.org/10.3390/metabo9100221

Ejemplares similares