Low Frequency of Heterozygous Deletion and Duplication in the MECP2 gene in Portuguese Patients with Rett Syndrome Artigo Académico uri icon

autores

  • Patrícia Espinheira de Sá Maciel
  • Shi, J.
  • Shibayama, A.
  • Liu, Q.
  • Nguyen, VQ.
  • Feng, J.
  • Temudo, T.
  • Maciel, P.
  • Sommer, SS.

data de publicação

  • janeiro 1, 2005