van Bon, B W M <br/><br/>
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID.  [electronic resource] 

 -  Molecular psychiatry  Jan 2016 
 - 126-32 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5578 
<br/><br/><label>Standard No.: </label>10.1038/mp.2015.5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Autistic Disorder--genetics<br/>Child<br/>Child, Preschool<br/>Cohort Studies<br/>Female<br/>Fetal Growth Retardation--genetics<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Microcephaly--genetics<br/>Middle Aged<br/>Mutation<br/>Phenotype<br/>Protein Serine-Threonine Kinases--genetics<br/>Protein-Tyrosine Kinases--genetics<br/>Seizures, Febrile--genetics<br/>Siblings<br/>Speech Disorders--genetics<br/>Stereotypic Movement Disorder--genetics<br/>Syndrome<br/>Young Adult<br/>Dyrk Kinases