Association of the Missense Variant p.Arg203Trp in PACS1 as a Cause of Intellectual Disability and Seizures

Authors

Diana Stern
Brooke Spangler
Nelly Oundjian
David Kronn, New York Medical CollegeFollow
Nandini Chandy, New York Medical CollegeFollow
Berivan Baskin
Wendy Chung

DOI

10.1111/cge.12956

Journal Title

Clinical Genetics

First Page

221

Last Page

223

Document Type

Article

Publication Date

8-1-2017

Department

Pediatrics

Keywords

ADHD, attention deficit hyperactivity disorder; ASD, atrial septal defect; DD, developmental delay; EEG, electroencephalogram; Ht, height; ID, intellectual disability; OCD, obsessive-compulsive disorder; OFC, open fontanelle; PDA, patent ductus arteriosis; PFO, patent foramen ovale; VSD, ventricular septal defect; Wt, weight.

Disciplines

Medicine and Health Sciences | Psychiatry and Psychology

Comments

Please see the work itself for the complete list of authors.

Recommended Citation

Stern, D., Spangler, B., Oundjian, N., Kronn, D., Chandy, N., Baskin, B., & Chung, W. (2017). Association of the Missense Variant p.Arg203Trp in PACS1 as a Cause of Intellectual Disability and Seizures. Clinical Genetics, 92 (2), 221-223. https://doi.org/10.1111/cge.12956

Publisher's Statement

Originally published in Clinical Genetics, 92 (2), 221-223. The original material can be found here.