Powis, Z <br/><br/>
De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms.  [electronic resource] 

 -  Clinical genetics  05 2018 
 - 1030-1038 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/cge.13198  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Autism Spectrum Disorder--genetics<br/>Child<br/>Child, Preschool<br/>Developmental Disabilities--genetics<br/>Female<br/>Genetic Predisposition to Disease<br/>Haploinsufficiency--genetics<br/>Humans<br/>Intellectual Disability--genetics<br/>Kruppel-Like Transcription Factors--genetics<br/>Male<br/>Mutation, Missense--genetics<br/>Exome Sequencing