TY - JOUR
T1 - Erratum
T2 - 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))
AU - University of Washington Center for Mendelian Genomics
AU - Sobering, Andrew K.
AU - Bryant, Laura M.
AU - Li, Dong
AU - McGaughran, Julie
AU - Maystadt, Isabelle
AU - Moortgat, Stephanie
AU - Graham, John M.
AU - van Haeringen, Arie
AU - Ruivenkamp, Claudia
AU - Cuperus, Roos
AU - Vogt, Julie
AU - Morton, Jenny
AU - Brasch-Andersen, Charlotte
AU - Steenhof, Maria
AU - Hansen, Lars Kjærsgaard
AU - Adler, Élodie
AU - Lyonnet, Stanislas
AU - Pingault, Veronique
AU - Sandrine, Marlin
AU - Ziegler, Alban
AU - Donald, Tyhiesia
AU - Nelson, Beverly
AU - Holt, Brandon
AU - Petryna, Oleksandra
AU - Firth, Helen
AU - McWalter, Kirsty
AU - Zyskind, Jacob
AU - Telegrafi, Aida
AU - Juusola, Jane
AU - Person, Richard
AU - Bamshad, Michael J.
AU - Earl, Dawn
AU - Chun-Hui Tsai, Anne
AU - Yearwood, Katherine R.
AU - Marco, Elysa
AU - Nowak, Catherine
AU - Douglas, Jessica
AU - Hakonarson, Hakon
AU - Bhoj, Elizabeth J.
N1 - Publisher Copyright:
© 2022 The Author(s)
PY - 2023/1/12
Y1 - 2023/1/12
N2 - (Human Genetics and Genomics Advances 3, 100102; July 14, 2022) The variant description c.1030C>T p.(Gln343∗) should have been c.1027C>T p.(Gln343∗) three times in the originally published version of this article. In Table 1 for variant 5 (individuals 6, 7, and 8), in Figure 5, and for individuals 6, 7, and 8 in Table S1. The article has been corrected online. The authors regret the errors.
AB - (Human Genetics and Genomics Advances 3, 100102; July 14, 2022) The variant description c.1030C>T p.(Gln343∗) should have been c.1027C>T p.(Gln343∗) three times in the originally published version of this article. In Table 1 for variant 5 (individuals 6, 7, and 8), in Figure 5, and for individuals 6, 7, and 8 in Table S1. The article has been corrected online. The authors regret the errors.
UR - http://www.scopus.com/inward/record.url?scp=85144484476&partnerID=8YFLogxK
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U2 - 10.1016/j.xhgg.2022.100168
DO - 10.1016/j.xhgg.2022.100168
M3 - Comment/debate
AN - SCOPUS:85144484476
SN - 2666-2477
VL - 4
JO - Human Genetics and Genomics Advances
JF - Human Genetics and Genomics Advances
IS - 1
M1 - 100168
ER -