Analysis of Highly Conserved Regions of the 3’UTR of MECP2 Gene in Patients with Clinical Diagnosis of Rett Syndrome and Other Disorders Associated with Mental Retardation

In this work we explored the role of the 3’UTR of the MECP2 gene in patients with clinical diagnosis of RTT and mental retardation; focusing on regions of the 3’UTR with almost 100% conservation at the nucleotide level among mouse and human. By mutation scanning (DOVAM-S technique) the MECP2 3’UTR o...

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Detalles Bibliográficos
Autores principales: Santos, Mónica, Yan, Jin, Temudo, Teresa, Oliveira, Guiomar, Vieira, José Pedro, Fen, Jinong, Sommer, Steve, Maciel, Patrícia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2008
Materias:
Other
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850630/
https://www.ncbi.nlm.nih.gov/pubmed/18688080
http://dx.doi.org/10.1155/2008/738401

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850630/
https://www.ncbi.nlm.nih.gov/pubmed/18688080
http://dx.doi.org/10.1155/2008/738401

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