Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))

Care4Rare Canada Consortium, Undiagnosed Diseases Network, Sureni V. Mullegama, Kaitlyn A. Kiernan, Erin Torti, Ethan Pavlovsky, Nicholas Tilton, Austin Sekula, Hua Gao, Joseph T. Alaimo, Kendra Engleman, Eric T. Rush, Karli Blocker, Katrina M. Dipple, Veronica M. Fettig, Heather Hare, Ian Glass, Dorothy K. Grange, Michael Griffin, Chanika PhornphutkulLauren Massingham, Lakshmi Mehta, Danny E. Miller, Jenny Thies, J. Lawrence Merritt, Eric Muller, Matthew Osmond, Sarah L. Sawyer, Rachel Slaugh, Rachel E. Hickey, Barry Wolf, Sanjeev Choudhary, Miljan Simonović, Yueqing Zhang, Timothy Blake Palculict, Aida Telegrafi, Deanna Alexis Carere, Ingrid M. Wentzensen, Michelle M. Morrow, Kristin G. Monaghan, Jane Juusola, Jun Yang

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Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology