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Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland

  • Irma Järvelä*
  • , Tuomo Määttä
  • , Anushree Acharya
  • , Juha Leppälä
  • , Shalini N. Jhangiani
  • , Maria Arvio
  • , Auli Siren
  • , Minna Kankuri-Tammilehto
  • , Hannaleena Kokkonen
  • , Maarit Palomäki
  • , Teppo Varilo
  • , Mary Fang
  • , Trevor D. Hadley
  • , Angad Jolly
  • , Tarja Linnankivi
  • , Ritva Paetau
  • , Anni Saarela
  • , Reetta Kälviäinen
  • , Jan Olme
  • , Liz M. Nouel-Saied
    • Diana M. Cornejo-Sanchez, Lorida Llaci, James R. Lupski, Jennifer E. Posey, Suzanne M. Leal, Isabelle Schrauwen
*Corresponding author for this work

    Research output: Contribution to journal › Article › Scientific › peer-review

    40 Citations (Scopus)
    25 Downloads (Pure)

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    Biochemistry, Genetics and Molecular Biology