Corrigendum to: Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms (American Journal of Medical Genetics Part A, (2018), 176, 2, (290-300), 10.1002/ajmg.a.38540)

C. M. Clarke, V. T. Fok, J. A. Gustafson, M. D. Smyth, A. E. Timms, C. D. Frazar, J. D. Smith, C. B. Birgfeld, A. Lee, R. G. Ellenbogen, J. S. Gruss, R. A. Hopper, M. L. Cunningham

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3 Scopus citations

Abstract

DOI: 10.1002/ajmg.a.38540 After publishing this manuscript two data errors were identified. Neither error affects the interpretation of the data. Table 3 lists three patients with TCF12 variants. Proband 95628 is listed as a female with a c.1907A>G; p.(Lys636Arg) variant. This proband is male, not female. This proband is correctly listed as a male in Supplemental Table S1a. Table 4 and Supplemental Table S1b list four probands with SCARF2 variants. Proband 95585 is inaccurately listed as having c.2593dupG: p.Ala865Serfs*184. The correct variant designation is c.2596dupG: p.Ala866Glyfs*191.

Original languageEnglish
Pages (from-to)2522
Number of pages1
JournalAmerican Journal of Medical Genetics, Part A
Volume176
Issue number11
DOIs
StatePublished - Nov 2018

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