학술논문
Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland
Document Type
article
Author
Mitja I. Kurki; Elmo Saarentaus; Olli Pietiläinen; Padhraig Gormley; Dennis Lal; Sini Kerminen; Minna Torniainen-Holm; Eija Hämäläinen; Elisa Rahikkala; Riikka Keski-Filppula; Merja Rauhala; Satu Korpi-Heikkilä; Jonna Komulainen–Ebrahim; Heli Helander; Päivi Vieira; Minna Männikkö; Markku Peltonen; Aki S. Havulinna; Veikko Salomaa; Matti Pirinen; Jaana Suvisaari; Jukka S. Moilanen; Jarmo Körkkö; Outi Kuismin; Mark J. Daly; Aarno Palotie
Source
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
Subject
Language
English
ISSN
2041-1723
Abstract
Various types of genetic variation contribute to the etiology of intellectual disability (ID). Here, the authors study a cohort of ID patients enriched for mild ID from Finland, to investigate contributions of rare and common variants associated with ID of different levels of severity.