TY  - GEN
AU  - Carrascosa-Romero, Mª Carmen
AU  - Barros-Angueira, Francisco
AU  - Castillo-Serrano, Ana
AU  - Fernández-Córdoba, Mª Sol
AU  - Sorli García, Moisés
AU  - Quintanilla-Mata, Mª Luisa
PY  - 2009
SN  - 0210–3893
UR  - http://hdl.handle.net/20.500.12105/14059
AB  - Mowat-Wilson syndrome –MWS- (MIM 235730) is a genetic condition caused by heterozygous mutations or deletions of the ZEB2 (Zinc finger E-box-binding homeobox 2 gene) gene, that codifies the SIP1 (Smad interacting protein 1) localized within the...
LA  - spa
PB  - Instituto de Salud Carlos III (ISCIII). Instituto de Investigación de Enfermedades Raras (IIER)
TI  - Síndrome de Mowat-Wilson con una deleción en el gen ZEB2 no descrita previamente
T2  - Mowat-Wilson Syndrome with a deletion of the ZEB2 gene previously undescribed
TY  - research article
ER  -