Alterations in the carnitine cycle in a mouse model of Rett syndrome

Rett syndrome (RTT) is a neurodevelopmental disease that leads to intellectual deficit, motor disability, epilepsy and increased risk of sudden death. Although in up to 95% of cases this disease is caused by de novo loss-of-function mutations in the X-linked methyl-CpG binding protein 2 gene, it is...

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Detalles Bibliográficos
Autores principales: Mucerino, Sabrina, Di Salle, Anna, Alessio, Nicola, Margarucci, Sabrina, Nicolai, Raffaella, Melone, Mariarosa A. B., Galderisi, Umberto, Peluso, Gianfranco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288798/
https://www.ncbi.nlm.nih.gov/pubmed/28150739
http://dx.doi.org/10.1038/srep41824

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288798/
https://www.ncbi.nlm.nih.gov/pubmed/28150739
http://dx.doi.org/10.1038/srep41824

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