All instances of ΧΛΔΝ19 should be read as CLDN19 throughout the "Materials and Methods" and "Results" sections.
Citation: Claverie-Martín F, García-Nieto V, Loris C, Ariceta G, Nadal I, Espinosa L, et al. (2013) Correction: Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis. PLoS ONE 8(10): 10.1371/annotation/25732fb0-ae38-40f6-b8c6-eb4ba94ac996. https://doi.org/10.1371/annotation/25732fb0-ae38-40f6-b8c6-eb4ba94ac996
Published: October 4, 2013
Copyright: © 2013 . This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Competing interests: No competing interests declared.