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

Added 220 days ago (28.04.2021)
Authors: 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
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