Correction to: Wide Spectrum of DUOX2 Deficiency: From Life-Threatening Compressive Goiter in Infancy to Lifelong Euthyroidism by Dufort G,Larrivée-Vanier S,Eugène D,De Deken X,Seebauer B,Heinimann K,Lévesque S,Gravel S,Szinnai G,Van Vliet G,and Deladoëy J. Thyroid 2019;29:1018–1022. DOI: 10.1089/thy.2018.0461

In the July 2019 issue of Thyroid (vol. 29, no. 7; 1018–1022) the article entitled “Wide Spectrum of DUOX2 Deficiency: From Life-Threatening Compressive Goiter in Infancy to Lifelong Euthyroidism” by Dufort et al. requires correction.

The length of the novel deletion reported on page 1019 was incorrect. The original data read:

Patient 1 harbored a previously described missense mutation (p.G1518S) known to abolish DUOX2 activity (2), as well as a novel 540 base-pair deletion spanning from intron 5 to exon 7 (NM_014080.4:c.513 + 53_818del, expected to be deleterious). No other variants were found by exome sequencing.

The data has been revised to:

Patient 1 harbored a previously described missense mutation (p.G1518S) known to abolish DUOX2 activity (2), as well as a novel 541 base-pair deletion spanning from intron 5 to exon 7 (NM_014080.4:c.513 + 53_818del, expected to be deleterious). No other variants were found by exome sequencing.

The online version of the article has been corrected to reflect this. The authors apologize for the error.