MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients

Mutations in the coding sequence of the methyl-CpG-binding protein 2 gene (MECP2), which cause Rett syndrome (RTT), have been found in male and female autistic subjects without, however, a causal relation having unequivocally been established. In this study, the MECP2 gene was scanned in a Portugues...

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Detalhes bibliográficos
Autor principal: Coutinho, A.M. (author)
Outros Autores: Oliveira, G. (author), Katz, C. (author), Feng, J. (author), Yan, J. (author), Yang, C. (author), Marques, C. (author), Ataíde, A. (author), Miguel, T.S. (author), Borges, L. (author), Almeida, J. (author), Correia, C. (author), Currais, A. (author), Bento, C. (author), Mota-Vieira, L. (author), Temudo, T. (author), Santos, M. (author), Maciel, P. (author), Sommer, S.S. (author), Vicente, A.M. (author)
Formato: article
Idioma:eng
Publicado em: 2011
Assuntos:
Autism
MECP2
3′UTR
Exon 1
Detection of Virtually All Mutations-SSCP
Perturbações do Desenvolvimento Infantil e Saúde Mental
Texto completo:http://hdl.handle.net/10400.18/322
País:Portugal
Oai:oai:repositorio.insa.pt:10400.18/322

Texto Completo

http://hdl.handle.net/10400.18/322

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