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Analysis of exonic deletions in a large population study provides novel insights into NRXN1 pathology

Title: Analysis of exonic deletions in a large population study provides novel insights into NRXN1 pathology
Authors: Montalbano, SimoneAff1, Aff2; Krebs, Morten DybdahlAff1, Aff2; Rosengren, AndersAff1, Aff2; Vaez, MortezaAff1, Aff2; Hellberg, Kajsa-Lotta GeorgiiAff1, Aff2; Mortensen, Preben B.Aff2, Aff3; Børglum, Anders D.Aff2, Aff4, Aff5; Geschwind, Daniel H.Aff6, Aff7, Aff8, Aff9; Raznahan, ArminAff10; Thompson, Wesley K.Aff2, Aff11; Helenius, DorteAff1, Aff2; Werge, ThomasAff1, Aff2, Aff12; Ingason, AndrésAff1, Aff2, IDs41525024004508_cor1; Hougaard, David M.Aff13; Nordentoft, MereteAff14; Mors, OleAff15; Grove, JakobAff2, Aff4, Aff5, Aff16; Als, Thomas D.Aff2, Aff4, Aff5; Buil, AlfonsoAff1, Aff2; Schork, Andrew J.Aff1, Aff2; Gådin, JesperAff1; Zetterberg, RichardAff1; Appadurai, VivekAff1; Meijsen, JoeriAff1; Vilhjálmsson, Bjarni J.Aff3, Aff16; Pedersen, Carsten B.Aff3; Agerbo, EsbenAff3; Christensen, JakobAff3; Petersen, Liselotte V.Aff3; Pedersen, Marianne GiørtzAff3; Bybjerg-Grauholm, JonasAff13; Bækvad-Hansen, MarieAff13
Source: npj Genomic Medicine. 9(1)
Database: Springer Nature Journals