학술논문
Erratum: Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology (Human Genetics and Genomics Advances (2022) 3(3), (S2666247722000185), (10.1016/j.xhgg.2022.100102))
Document Type
Erratum
Author
Sobering, A.K.; Bryant, L.M.; Li, D.; McGaughran, J.; Maystadt, I.; Moortgat, S.; Graham, J.M.; van Haeringen, A.; Ruivenkamp, C.; Cuperus, R.; Vogt, J.; Morton, J.; Brasch-Andersen, C.; Steenhof, M.; Hansen, L.K.; Adler, É.; Lyonnet, S.; Pingault, V.; Sandrine, M.; Ziegler, A.; Donald, T.; Nelson, B.; Holt, B.; Petryna, O.; Firth, H.; McWalter, K.; Zyskind, J.; Telegrafi, A.; Juusola, J.; Person, R.; Bamshad, M.J.; Earl, D.; Chun-Hui Tsai, A.; Yearwood, K.R.; Marco, E.; Nowak, C.; Douglas, J.; Hakonarson, H.; Bhoj, E.J.
Source
In: Human Genetics and Genomics Advances . (Human Genetics and Genomics Advances, 12 January 2023, 4(1))
Subject
Language
English
ISSN
26662477