학술논문
De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features
Document Type
Article
Author
Mullegama, S.V.; Torti, E.; Gao, H.; Palculict, T.B.; Telegrafi, A.; Carere, D.A.; Wentzensen, I.M.; Morrow, M.M.; Monaghan, K.G.; Juusola, J.; Pavlovsky, E.; Tilton, N.; Sekula, A.; Griffin, M.; Choudhary, S.; Kiernan, K.A.; Simonović, M.; Alaimo, J.T.; Engleman, K.; Rush, E.T.; Blocker, K.; Muller, E.; Dipple, K.M.; Glass, I.; Miller, D.E.; Merritt, J.L.; Fettig, V.M.; Hare, H.; Grange, D.K.; Slaugh, R.; Phornphutkul, C.; Massingham, L.; Mehta, L.; Thies, J.; Osmond, M.; Sawyer, S.L.; Hickey, R.E.; Wolf, B.; Zhang, Y.; Yang, J.
Source
In: American Journal of Human Genetics . (American Journal of Human Genetics, 4 April 2024, 111(4):778-790)
Subject
Language
English
ISSN
15376605
00029297
00029297