Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes

Rett syndrome (RTT) is a rare disease but still one of the most abundant causes for intellectual disability in females. Typical symptoms are onset at month 6–18 after normal pre- and postnatal development, loss of acquired skills and severe intellectual disability. The type and severity of symptoms...

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Detalles Bibliográficos
Autores principales: Ehrhart, Friederike, Coort, Susan L. M., Cirillo, Elisa, Smeets, Eric, Evelo, Chris T., Curfs, Leopold M. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123333/
https://www.ncbi.nlm.nih.gov/pubmed/27884167
http://dx.doi.org/10.1186/s13023-016-0545-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5123333/
https://www.ncbi.nlm.nih.gov/pubmed/27884167
http://dx.doi.org/10.1186/s13023-016-0545-5

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