TY - JOUR
T1 - Correction to
T2 - Park et al. Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis. J. Clin. Med. 2020, 9, 2013
AU - Park, Eujin
AU - Lee, Chung
AU - Kim, Nayoung K.D.
AU - Ahn, Yo Han
AU - Park, Young Seo
AU - Lee, Joo Hoon
AU - Kim, Seong Heon
AU - Cho, Min Hyun
AU - Cho, Heeyeon
AU - Yoo, Kee Hwan
AU - Shin, Jae Il
AU - Kang, Hee Gyung
AU - Ha, Il Soo
AU - Park, Woong Yang
AU - Cheong, Hae Il
N1 - Publisher Copyright:
© The Authors.
PY - 2022/6/1
Y1 - 2022/6/1
N2 - 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).”.
AB - 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).”.
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U2 - 10.3390/jcm11113016
DO - 10.3390/jcm11113016
M3 - Comment/debate
AN - SCOPUS:85130817500
SN - 2077-0383
VL - 11
JO - Journal of Clinical Medicine
JF - Journal of Clinical Medicine
IS - 11
M1 - 3016
ER -