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. uri icon

autores

  • Patrícia Espinheira de Sá Maciel
  • Santos, M.
  • Yan, J.
  • Temudo, T.
  • Oliveira, G.
  • Vieira, J.P.
  • Fen, J.
  • Sommer, S.
  • Maciel, P.

data de publicação

  • janeiro 1, 2008