Errors in End Matter. In the Ophthalmic Molecular Genetics article titled “Evidence for Keratoconus Susceptibility Locus on Chromosome 14: A Genome-wide Linkage Screen Using Single-Nucleotide Polymorphism Markers” by Liskova et al, published in the September issue of the Archives (2010;128:1191-1195), 2 sections of end matter were accidently omitted. There should have been an Author Contributions section that read “Drs Liskova and Hysi contributed equally to this work. Drs Liskova and Hysi had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.” and an Additional Contributions section that read “Quincy Prescott, MSc (Institute of Ophthalmology, University College London), provided technical support for the project and Kerra Pearce (UCL Genomics) assisted with sample processing. We thank Alison J. Hardcastle (Institute of Ophthalmology, University College London) for valuable comments on the study design.”
Errors in End Matter in: Evidence for Keratoconus Susceptibility Locus on Chromosome 14: A Genome-wide Linkage Screen Using Single-Nucleotide Polymorphism Markers. Arch Ophthalmol. 2010;128(11):1431. doi:10.1001/archophthalmol.2010.247
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