Immune Dysfunction in Rett Syndrome Patients Revealed by High Levels of Serum Anti-N(Glc) IgM Antibody Fraction

Rett syndrome (RTT), a neurodevelopmental disorder affecting exclusively (99%) female infants, is associated with loss-of-function mutations in the gene encoding methyl-CpG binding protein 2 (MECP2) and, more rarely, cyclin-dependent kinase-like 5 (CDKL5) and forkhead box protein G1 (FOXG1). In this...

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Detalles Bibliográficos
Autores principales: Papini, Anna Maria, Nuti, Francesca, Real-Fernandez, Feliciana, Rossi, Giada, Tiberi, Caterina, Sabatino, Giuseppina, Pandey, Shashank, Leoncini, Silvia, Signorini, Cinzia, Pecorelli, Alessandra, Guerranti, Roberto, Lavielle, Solange, Ciccoli, Lucia, Rovero, Paolo, De Felice, Claudio, Hayek, Joussef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214166/
https://www.ncbi.nlm.nih.gov/pubmed/25389532
http://dx.doi.org/10.1155/2014/260973

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214166/
https://www.ncbi.nlm.nih.gov/pubmed/25389532
http://dx.doi.org/10.1155/2014/260973

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