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 Palomaki, Teppo Varilo, Mary Fang, Trevor D. Hadley, Angad Jolly, Tarja Linnankivi, Ritva Paetau, Anni Saarela, Reetta Kalviainen, Jan Olme, Liz M. Nouel-SaiedDiana M. Cornejo-Sanchez, Lorida Llaci, James R. Lupski, Jennifer E. Posey, Suzanne M. Leal, Isabelle Schrauwen

Forskningsoutput: TidskriftsbidragArtikelPeer review

Originalspråkengelska
TidskriftHuman Genetics
Antal sidor19
ISSN0340-6717
DOI
Status!!E-pub ahead of print - 12 mar 2021
MoE-publikationstypA1 Tidskriftsartikel-refererad

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