Cordelli, Duccio Maria <br/><br/>
Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype.  [electronic resource] 

 -  American journal of medical genetics. Part A  Feb 2013 
 - 273-84 p.  digital 
<br/><br/> Publication Type: Journal Article; Multicenter Study 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.35717  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Anticonvulsants--therapeutic use<br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Electroencephalography<br/>Facies<br/>Female<br/>Hirschsprung Disease--drug therapy<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Intellectual Disability--drug therapy<br/>Male<br/>Microcephaly--drug therapy<br/>Mutation<br/>Phenotype<br/>Repressor Proteins--genetics<br/>Retrospective Studies<br/>Seizures--drug therapy<br/>Valproic Acid--therapeutic use<br/>Young Adult<br/>Zinc Finger E-box Binding Homeobox 2