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))

University of Washington Center for Mendelian Genomics

Research output: Contribution to journalComment/debatepeer-review

1 Scopus citations

Abstract

(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.

Original languageEnglish (US)
Article number100168
JournalHuman Genetics and Genomics Advances
Volume4
Issue number1
DOIs
StatePublished - Jan 12 2023

ASJC Scopus subject areas

  • Molecular Medicine
  • Genetics(clinical)

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