Human CRY1 variants associate with attention deficit/hyperactivity disorder

Attention deficit/hyperactivity disorder (ADHD) is a common and heritable phenotype frequently accompanied by insomnia, anxiety, and depression. Here, using a reverse phenotyping approach, we report heterozygous coding variations in the core circadian clock gene cryptochrome 1 in 15 unrelated multig...

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Dades bibliogràfiques
Publicat a:J Clin Invest
Autors principals: Onat, O. Emre, Kars, M. Ece, Gül, Şeref, Bilguvar, Kaya, Wu, Yiming, Özhan, Ayşe, Aydın, Cihan, Başak, A. Nazlı, Trusso, M. Allegra, Goracci, Arianna, Fallerini, Chiara, Renieri, Alessandra, Casanova, Jean-Laurent, Itan, Yuval, Atbaşoğlu, Cem E., Saka, Meram C., Kavaklı, İ. Halil, Özçelik, Tayfun
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 2020
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7324179/
https://ncbi.nlm.nih.gov/pubmed/32538895
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI135500
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