Characterizing Sleep Problems in 16p11.2 Deletion and Duplication

Studies of 16p11.2 copy number variants (CNVs) provide an avenue to identify mechanisms of impairment and develop targeted treatments for individuals with neurodevelopmental disorders. 16p11.2 deletion and duplication phenotypes are currently being ascertained; however, sleep disturbances are minima...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Journal of autism and developmental disorders 2023-04, Vol.53 (4), p.1462-1475
Hauptverfasser:	Kamara, Dana, De Boeck, Paul, Lecavalier, Luc, Neuhaus, Emily, Beauchaine, Theodore P.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adults Analysis Autism Autism Spectrum Disorder - genetics Autistic Disorder - genetics Behavioral Science and Psychology Bipolar disorder Carriers Child and School Psychology Chromosome Deletion Chromosomes, Human, Pair 16 - genetics Circadian rhythm Complications and side effects Copy number Copy number variations Demographic aspects Diagnosis DNA Copy Number Variations - genetics Duplication Factor analysis Genetic Disorders Genetics Humans Intellectual Disability - genetics Neurodevelopmental disorders Neurodevelopmental Disorders - genetics Neurosciences Original Paper Pediatrics Pervasive developmental disorders Phenotype Phenotypes Problems Psychology Public Health Relatives Risk factors Sleep Sleep disorders Teenagers Variants Youth
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!