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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 Feuk
Published 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.
Keyphrases
  • intellectual disability
  • genome wide
  • autism spectrum disorder
  • copy number
  • dna methylation
  • risk factors
  • circulating tumor
  • single molecule
  • gene expression
  • human immunodeficiency virus