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. 2018 Dec 6;103(6):1054–1055. doi: 10.1016/j.ajhg.2018.11.009

Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features

Peter D Turnpenny ∗, Michael J Wright, Melissa Sloman, Richard Caswell, Anthony J van Essen, Erica Gerkes, Rolph Pfundt, Susan M White, Nava Shaul-Lotan, Lori Carpenter, G Bradley Schaefer, Alan Fryer, A Micheil Innes, Kirsten P Forbes, Wendy K Chung, Heather McLaughlin, Lindsay B Henderson, Amy E Roberts, Karen E Heath, Beatriz Paumard-Hernández, Blanca Gener; the DDD study, Katherine A Fawcett, Romana Gjergja-Juraški, Daniela T Pilz, Andrew E Fry ∗∗
PMCID: PMC6288271  PMID: 30526864

(The American Journal of Human Genetics 103, 786–793; November 1, 2018)

Main Text

The gender symbol for individual 6 in Figure 1 is incorrect. This individual is female, not male. The corrected figure appears here and online, and the authors regret the error.

Figure 1.

Figure 1

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Facial Features of Individuals with PCGF2 Mutations (Corrected)

Figure 1.

Figure 1

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Facial Features of Individuals with PCGF2 Mutations (Original)

Contributor Information

Peter D. Turnpenny, Email: peter.turnpenny@nhs.net.

Andrew E. Fry, Email: fryae@cardiff.ac.uk.

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

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