Figures
The images for Figs. 1 and 2 are incorrectly switched. The image that appears as Fig 1 should be Fig 2, and the image that appears as Fig 2 should be Fig 1. The figure captions appear in the correct order.
Vertical lines in bold at -2 SD and +2 SD indicate the reference range for leptin SDS. As a consequence, lower motor function is linked to high leptin-SDS independent of SMA type.
Vertical lines in bold (- 2 SD, + 2 SD) indicate the reference range. Boxes indicate the interquartile range (IQR), whiskers indicate 1.5xIQR, black dots are outliers. Asterisks indicate a significant deviation of the median from zero (p <0.01) with a shift towards higher values for WHR and leptin, as well as a shift to lower values for weight, height, BMI und HC.
Reference
Citation: Kölbel H, Hauffa BP, Wudy SA, Bouikidis A, Della Marina A, Schara U (2017) Correction: Hyperleptinemia in children with autosomal recessive spinal muscular atrophy type I-III. PLoS ONE 12(4): e0175611. https://doi.org/10.1371/journal.pone.0175611
Published: April 6, 2017
Copyright: © 2017 Kölbel et al. 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.