Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome
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R. Pfundt | M. Reijnders | D. Schubert | I. Thiffault | V. Tasic | J. Wheless | C. Gilissen | T. Kleefstra | M. Schepens | A. Rauch | Jamie M. Kramer | P. Joset | O. Bodamer | Deniz Top | A. Raas-Rothschild | M. Willemsen | M. Sinnema | P. Agrawal | D. Koolen | M. Cho | K. V. van Gassen | P. Terhal | C. Genetti | K. Steindl | J. Hoefele | J. van der Smagt | Marleen E. H. Simon | Diante E Stremmelaar | A. Casey | K. McWalter | K. Riedhammer | Angela Bahr | Dihong Zhou | M. Ruiterkamp-Versteeg | T. Hoffman | Joost Kummeling | N. Raun | Calvin C. O. Man | E. Keller | N. Powell-Hamilton | K. Engleman | Eva M C Schwaibold | M. Higgs | Eva M. C. Schwaibold | A. Raas‐Rothschild | Nicholas Raun | D. E. Stremmelaar | Margot R. F. Reijnders | Kendra L. Engleman
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