Erratam to novel SOX2 mutations and genotype-phenotype correlation in anophthalmia and microphthalmia

Authors

  • Adele Schneider,

  • Tanya Bardakjian,

  • Linda M. Reis,

  • Rebecca C. Tyler,

  • Elena V. Semina

    Corresponding author
    • C3520, Translational and Biomedical Research Center, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, Wisconsin 53226.
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Errata

This article corrects:


    • How to Cite this Article: Schneider A, Bardakjian T, Reis LM, Tyler RC, Semina EV. 2012. Erratum to novel SOX2 mutations and genotype-phenotype correlation in anophthalmia and microphthalmia. Am J Med Genet Part A 158A:267.

    In the article entitled “Novel SOX2 Mutations and Genotype-Phenotype Correlation in Anophthalmia and Microphthalmia” by Schneider et al. [Am J Med Genet 149A:2706–2715], in Table II there was an error in the assignment of the abbreviations EA (esophageal atresia) and EN (endocrine anomalies).

    The following patients have EA: c.60insG, c.70del17(1), c.70del20(2), c.163C>T, Deletion(6), and c.221G>C. The following patients have EN: c.53C>A, c.60insG, c.70del20(4), c.70del20(7), c.181C>T, c.387delC, c.479delA, c.480insA, c.487ins2, c.529c>T(3), e.551delC(1), c.551delC(2), c.69ins3, Deletion(1), Deletion(4), Deletion(8), c.224T>A, and c.571G>A.

    The authors apologize for the errors.

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