Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family.
Eva Lindholm CarlströmJonatan HalvardsonMitra EtemadikhahLennart WetterbergKarl-Henrik GustavsonLars FeukPublished in: BMC medical genomics (2019)
DNA samples from the large family analyzed in this study were initially collected based on a hypothesis that affected members shared a major genetic risk factor. Our results show that a complex phenotype such as mild intellectual disability in large families from genetically isolated populations may show considerable genetic heterogeneity.