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Erratum: Clinical, radiologic, and genetic features of Korean patients with Mucopolysaccharidosis IVA
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Clin Exp Pediatr > Volume 56(3); 2013
Lee, Cho, Maeng, Jeon, Sohn, Kim, Park, and Jin: Erratum: Clinical, radiologic, and genetic features of Korean patients with Mucopolysaccharidosis IVA

Correspondence

Erratum: Clinical, radiologic, and genetic features of Korean patients with Mucopolysaccharidosis IVA

Na Hee Lee, MD1, Sung Yoon Cho, MD1, Se Hyun Maeng, MD1, Tae Yeon Jeon, MD2, Young Bae Sohn, MD, PhD3, Su Jin Kim, MD, PhD4, Hyung-Doo Park, MD, PhD5, Dong Kyu Jin, MD, PhD1

1Department of Pediatrics, Samsung Medical Center, Sunkyunkwan University School of Medicine, Seoul, Korea.

2Department Radiology & Center for Imaging Science, Samsung Medical Center, Sunkyunkwan University School of Medicine, Seoul, Korea.

3Department of Medical Genetics, Ajou University School of Medicine, Suwon, Korea.

4Center of Pediatric Oncology, National Cancer Center, Goyang, Korea.

5Department of Laboratory Medicine & Genetics, Samsung Medical Center, Sunkyunkwan University School of Medicine, Seoul, Korea.

Copyright © 2013 by The Korean Pediatric Society

(open-access, http://creativecommons.org/licenses/by-nc/3.0/):

This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Korean Journal of Pediatrics 2013;56(3):143.

Published online: March 18, 2013

DOI: https://doi.org/10.3345/kjp.2013.56.3.143

To the Editor:
We found an error in our published article:
Lee NH, Cho SY, Maeng SH, Jeon TY, Sohn YB, Kim SJ, Park HD, Jin DK. Clinical, radiologic, and genetic features of Korean patients with Mucopolysaccharidosis IVA. Korean J Pediatr 2012;55:430-11. http://dx.doi.org/10.3345/kjp.2012.55.11.430
Page 435,
Nomenclature should be modified as follows:
One mutation of c.1568A>G (p.X523W) in patient 6 was a novel homozygous mutation. But we didn't have approval of family study in this patient.
Table 4 should be modified as follows:
kjped-56-143-i001.jpg
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