학술논문
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))
Document Type
Erratum
Author
Mullegama, S.V.; Kiernan, K.A.; Torti, E.; Pavlovsky, E.; Tilton, N.; Sekula, A.; Gao, H.; Alaimo, J.T.; Engleman, K.; Rush, E.T.; Blocker, K.; Dipple, K.M.; Fettig, V.M.; Hare, H.; Glass, I.; Grange, D.K.; Griffin, M.; Phornphutkul, C.; Massingham, L.; Mehta, L.; Miller, D.E.; Thies, J.; Merritt, J.L.; Muller, E.; Osmond, M.; Sawyer, S.L.; Slaugh, R.; Hickey, R.E.; Wolf, B.; Choudhary, S.; Simonović, M.; Zhang, Y.; Palculict, T.B.; Telegrafi, A.; Carere, D.A.; Wentzensen, I.M.; Morrow, M.M.; Monaghan, K.G.; Juusola, J.; Yang, J.
Source
In: American Journal of Human Genetics . (American Journal of Human Genetics, 6 June 2024, 111(6):1240)
Subject
Language
English
ISSN
15376605
00029297
00029297