Encontrados 2 documentos, a visualizar página 1 de 1
Ordenado por
Data
ir para a página:
1
MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients
Coutinho, A.M.; Oliveira, G.; Katz, C.; Feng, J.; Yan, J.; Yang, C.; Marques, C.; Ataíde, A.; Miguel, T.S.; Borges, L.; Almeida, J.; Correia, C.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 Portuguese autistic population, hypothesizing that the phenotypic spectrum of mutations extends beyond the traditional diag...
Data: 2007
|
Origem: Repositório Científico do Instituto Nacional de Saúde
Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric p...
Yan, J.; Oliveira, G.; Coutinho, A.; Yang, C.; Feng, J.; Katz, C.; Sram, J.; Bockholt, A.; Jones, I.R.; Craddock, N.; Cook Jr, E.H.; Vicente, A.
Data: 2005
|
Origem: Repositório Científico do Instituto Nacional de Saúde
| Financiadores do RCAAP | |||||||
|
|
|
|
|
|
||