| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8683729 | Epilepsy & Behavior | 2018 | 5 Pages |
Abstract
Caring for patients with DS exerts physical, emotional, and time burdens on caregivers. Supportive services for DS families are identified to highlight an unmet need for DS treatments.
Keywords
Related Topics
Life Sciences
Neuroscience
Behavioral Neuroscience
Authors
Jonathan D. Campbell, Melanie D. Whittington, Chong H. Kim, Gina R. VanderVeen, Kelly G. Knupp, Arnold Gammaitoni,