Erratum: Correction of Table: Genetic Mutation Profiles in Korean Patients with Inherited Retinal Diseases

Min Seok Kim; Kwangsic Joo; Moon-Woo Seong; Man Jin Kim; Kyu Hyung Park; Sung Sup Park; Se Joon Woo

doi:10.3346/jkms.2019.34.e245

Correspondence

Journal of Korean Medical Science 2019; 34(35): e245.

Published online: 3 September 2019

DOI: https://doi.org/10.3346/jkms.2019.34.e245

Erratum: Correction of Table: Genetic Mutation Profiles in Korean Patients with Inherited Retinal Diseases

Min Seok Kim^1,^*

, Kwangsic Joo^1,^*

, Moon-Woo Seong^2,^*

, Man Jin Kim²

, Kyu Hyung Park¹

, Sung Sup Park²

, Se Joon Woo¹

¹Department of Ophthalmology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.

²Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.

Address for Correspondence: Sung Sup Park, MD, PhD. Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, 101 Daehak-ro, Jongno-gu, Seoul 03080, Republic of Korea. sparkle@snu.ac.kr

Address for Correspondence: Se Joon Woo, MD, PhD. Department of Ophthalmology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, 82 Gumi-ro, 173-beon-gil, Bundang-gu, Seongnam 13620, Republic of Korea. sejoon1@snu.ac.kr

Equal contributor:

^*Min Seok Kim, Kwangsic Joo, and Moon-Woo Seong contributed equally to this work.

Received 31 August 2019 Accepted 3 September 2019

The Korean Academy of Medical Sciences

(open-access, https://creativecommons.org/licenses/by-nc/4.0/):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

To the Editor:

The authors regret that there were errors in Table 2 and Supplementary Table.

Thank you for your kind consideration.

The corrected notation is as follows:

1) In Table 2, the amino acid change detected in the first patient of Stargardt disease (p.D654N) should be changed to p.D645N.

2) In Supplementary Table, RefSeq-mRNA should be changed in BBS9 (from NM_001033604 to NM_198428.2), BEST1 (from NM_001139443 to NM_004183.3), CNGA3 (from NM_001079878 to NM_001298.2), PROM1 (from NM_001145847 to NM_006017.2), TRPM1 (from NM_002420 to NM_001252020.1)