Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis (vol 9, 2013, 2020)open access
- Authors
- Park, Eujin; Lee, Chung; Kim, Nayoung K. D.; Ahn, Yo Han; Park, Young Seo; Lee, Joo Hoon; Kim, Seong Heon; Cho, Min Hyun; Cho, Heeyeon; Yoo, Kee Hwan; Shin, Jae Il; Kang, Hee Gyung; Ha, Il-Soo; Park, Woong-Yang; Cheong, Hae Il
- Issue Date
- 6월-2022
- Publisher
- MDPI
- Citation
- JOURNAL OF CLINICAL MEDICINE, v.11, no.11
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF CLINICAL MEDICINE
- Volume
- 11
- Number
- 11
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/144116
- DOI
- 10.3390/jcm11113016
- ISSN
- 2077-0383
- Abstract
- In the original article [1], there were errors in Tables 2, 3 and S2 as published. The patient SRNS-168 was the only one having COQ2 mutations in the study. However, it was incorrectly described as a mutation in the COQ6 gene. The corrected Tables 2, 3 and S2 appear below. Also, the sentences in Abstract and Results Section 3.2. paragraph 2 have been corrected. “WT1 was the most common causative gene (23.6%), followed by COQ6 (8.7%), NPHS1 (8.7%), NUP107 (7.1%), and COQ8B (6.3%).” “WT1 was the most common causative gene (23.6%, 30 patients), followed by COQ6 (8.7%, 11 patients), NPHS1 (8.7%, 11 patients), NUP107 (7.1%, 9 patients), COQ8B (6.3%, 8 patients), MYH9 (4.7%, 6 patients), and INF2 (4.7%, 6 patients) (Table 2).”. © The Authors.
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