%0 Journal Article 
%T Mowat-Wilson'S Syndrome: A Case Report
%D 2012
%@ 0370-4106
%U http://hdl.handle.net/10906/81230
%X Mowat-Wilson syndrome (MWS) is a very infrequent congenital polimalformative disorder, caused by mutations, deletions or insertions of the ZEB2 gene, which codify for a protein that is involved in the migration of the neural crest cells and the development of middle line structures. The inheritance pattern is autosomal dominant, haplo-insufficient.

%K Ciencias socio biomédicas
%K Medical sciences
%K Enfermedad de Hirschsprung
%K Defectos congénitos
%K Epilepsia
%K Neurología pediátrica
%K Retardo mental
%K Cardiopatías congénitas
%~ GOEDOC, SUB GOETTINGEN