Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission

Several types of genetic alterations occurring at numerous loci have been described in attention deficit hyperactivity disorder (ADHD). However, the role of rare single nucleotide variants (SNVs) remains under investigated. Here, we sought to identify rare SNVs with predicted deleterious effect that...

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Detalles Bibliográficos
Autores principales: Al-Mubarak, Bashayer R., Omar, Aisha, Baz, Batoul, Al-Abdulaziz, Basma, Magrashi, Amna I., Al-Yemni, Eman, Jabaan, Amjad, Monies, Dorota, Abouelhoda, Mohamed, Abebe, Dejene, Ghaziuddin, Mohammad, Al-Tassan, Nada A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382449/
https://www.ncbi.nlm.nih.gov/pubmed/32238911
http://dx.doi.org/10.1038/s41431-020-0619-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7382449/
https://www.ncbi.nlm.nih.gov/pubmed/32238911
http://dx.doi.org/10.1038/s41431-020-0619-7

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