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  • the Korean Society for Brain and Neural Sciences

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Erratum

Exp Neurobiol 2020; 29(5): 402-402

Published online October 31, 2020

https://doi.org/10.5607/en20009e1

© The Korean Society for Brain and Neural Sciences

Development of a Laboratory-safe and Low-cost Detection Protocol for SARS-CoV-2 of the Coronavirus Disease 2019 (COVID-19)

Joungha Won, Solji Lee, Myungsun Park, Tai Young Kim, Mingu Gordon Park, Byung Yoon Choi, Dongwan Kim, Hyeshik Chang, Won Do Heo, V. Narry Kim and C. Justin Lee

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License
(http://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.

BODY

Exp Neurobiol. 2020 Apr;29(2):107-119. doi: 10.5607/en.20009. Epub 2020 Apr 30.

We would like to correct author’s affiliations, add an author and an edit one sentence as shown below.

1) The corrected affiliations (switch affiliation 1 and 2) and added author are marked by bold and underlines. Joungha Won1,2, Solji Lee2, Myungsun Park2, Tai Young Kim2, Mingu Gordon Park2,3, Byung Yoon Choi4, Dongwan Kim5,6, Hyeshik Chang5,6, Won Do Heo1, V. Narry Kim5,6 and C. Justin Lee2*

1Department of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, 2Center for Cognition and Sociality, Cognitive Glioscience Group, Institute for Basic Science, Daejeon 34126, 3KU-KIST Graduate School of Converging Science and Technology, Korea University, Seoul 02841, 4Department of Otorhinolaryngology, Seoul National University Bundang Hospital, Seongnam 13620, 5Center for RNA Research, Institute for Basic Science, Seoul 08826, 6School of Biological Sciences, Seoul National University, Seoul 08826, Korea

2) In Quantitative rtPCR section (Page 110, in material and methods) we would like to correct the following sentence from; “In brief, each reaction buffer consisted of a total volume of 20 μl containing 8 μl of 100 μM forward and reverse primers (4 μl for each primer), 2 μl of cDNA, and 10 μl power SYBR Green PCR Master Mix.”

to;

“In brief, each reaction buffer consisted of a total volume of 20 μl containing 2 μl of 10 μM forward and reverse primers (1 μl for each primer), 2 μl of cDNA, and 10 μl power SYBR Green PCR Master Mix.”