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. 2024 May 14;111(6):1240. doi: 10.1016/j.ajhg.2024.05.004

De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features

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 Phornphutkul, Lauren Massingham, Lakshmi Mehta, Danny E Miller, Jenny Thies, J Lawrence Merritt II, Eric Muller II, Matthew Osmond, Sarah L Sawyer, Rachel Slaugh, Rachel E Hickey, Barry Wolf; Care4Rare Canada Consortium; Undiagnosed Diseases Network, 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 ∗∗
PMCID: PMC11179398  PMID: 38749428

Main text

(The American Journal of Human Genetics 111, 778–790; April 4, 2024)

In the originally published version of the paper, the placement of the final two authors was incorrect. Both Jane Juusola and Jun Yang are co-senior authors; J.J. should appear second-to-last and J.Y. appear last.

The authors apologize for this error.

Contributor Information

Sureni V. Mullegama, Email: smullegama@genedx.com.

Jun Yang, Email: junyang@utmb.edu.

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

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