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Human Genetics and Genomics Advances logoLink to Human Genetics and Genomics Advances
. 2022 Dec 20;4(1):100168. doi: 10.1016/j.xhgg.2022.100168

Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology

Andrew K Sobering , Laura M Bryant, Dong Li, Julie McGaughran, Isabelle Maystadt, Stephanie Moortgat, John M Graham Jr, Arie van Haeringen, Claudia Ruivenkamp, Roos Cuperus, Julie Vogt, Jenny Morton, Charlotte Brasch-Andersen, Maria Steenhof, Lars Kjærsgaard Hansen, Élodie Adler, Stanislas Lyonnet, Veronique Pingault, Marlin Sandrine, Alban Ziegler, Tyhiesia Donald, Beverly Nelson, Brandon Holt, Oleksandra Petryna, Helen Firth, Kirsty McWalter, Jacob Zyskind, Aida Telegrafi, Jane Juusola, Richard Person, Michael J Bamshad, Dawn Earl; University of Washington Center for Mendelian Genomics, Anne Chun-Hui Tsai, Katherine R Yearwood, Elysa Marco, Catherine Nowak, Jessica Douglas, Hakon Hakonarson, Elizabeth J Bhoj ∗∗
PMCID: PMC9792386  PMID: 36583168

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(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.

Contributor Information

Andrew K. Sobering, Email: andrew.sobering@uga.edu.

Elizabeth J. Bhoj, Email: bhoje@chop.edu.


Articles from Human Genetics and Genomics Advances are provided here courtesy of Elsevier

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