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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Dades bibliogràfiques
Publicat a:Eur J Hum Genet
Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: Springer International Publishing 2020
Matèries:
Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7382449/
https://ncbi.nlm.nih.gov/pubmed/32238911
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41431-020-0619-7
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