Absence epilepsy and the CHD2 gene: an adolescent male with moderate intellectual disability, short-lasting psychoses, and an interstitial deletion in 15q26.1–q26.2

Autor: Willem M.A. Verhoeven, José Zuydam, Jos I. M. Egger, Alida C. Knegt, Tjitske Kleefstra

Publikováno v: Neuropsychiatric Disease and Treatment
Neuropsychiatric Disease and Treatment, 12, 1135-1139. Dove Medical Press Ltd.
Neuropsychiatric Disease and Treatment, 12, pp. 1135-1139
Neuropsychiatric Disease and Treatment, 12, 1135-1139

Contains fulltext : 167606.pdf (Publisher’s version ) (Open Access) Deletions of the 15q26 region encompassing the chromodomain helicase DNA binding domain 2 (CHD2) gene have been associated with intellectual disability, behavioral problems, and se

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e633dd946b96224d60cad8a35b9c5de5
http://europepmc.org/articles/PMC4869798