학술논문
Erratum: A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3 (The American Journal of Human Genetics (2024) 111(1) (96–118), (S0002929723004366), (10.1016/j.ajhg.2023.12.004))
Document Type
Erratum
Author
Paul, M.S.; Michener, S.L.; Pan, H.; Chan, H.; Pfliger, J.M.; Rosenfeld, J.A.; Lerma, V.C.; Tran, A.; Longley, M.A.; Lewis, R.A.; Weisz-Hubshman, M.; Bekheirnia, M.R.; Bekheirnia, N.; Massingham, L.; Zech, M.; Wagner, M.; Engels, H.; Cremer, K.; Mangold, E.; Peters, S.; Trautmann, J.; Perne, C.; Mester, J.L.; Guillen Sacoto, M.J.; Person, R.; McDonnell, P.P.; Cohen, S.R.; Lusk, L.; Cohen, A.S.A.; Le Pichon, J.-B.; Pastinen, T.; Zhou, D.; Engleman, K.; Racine, C.; Faivre, L.; Moutton, S.; Denommé-Pichon, A.-S.; Koh, H.Y.; Poduri, A.; Bolton, J.; Knopp, C.; Julia Suh, D.S.; Maier, A.; Toosi, M.B.; Karimiani, E.G.; Maroofian, R.; Schaefer, G.B.; Ramakumaran, V.; Vasudevan, P.; Banos-Pinero, B.; Pagnamenta, A.T.; Prasad, C.; Osmond, M.; Schuhmann, S.; Vasileiou, G.; Russ-Hall, S.; Scheffer, I.E.; Carvill, G.L.; Mefford, H.; Bacino, C.A.; Lee, B.H.; Chao (趙孝端), H.-T.
Source
In: American Journal of Human Genetics . (American Journal of Human Genetics, 6 June 2024, 111(6):1239)
Subject
Language
English
ISSN
15376605
00029297
00029297