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Author Correction: mRNA analysis identifies deep intronic variants causing Alport syndrome and overcomes the problem of negative results of exome sequencing
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8578218/ https://www.ncbi.nlm.nih.gov/pubmed/34754083 http://dx.doi.org/10.1038/s41598-021-01604-9 |
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author | Wang, Xiaoyuan Zhang, Yanqin Ding, Jie Wang, Fang |
author_facet | Wang, Xiaoyuan Zhang, Yanqin Ding, Jie Wang, Fang |
author_sort | Wang, Xiaoyuan |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-8578218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85782182021-11-10 Author Correction: mRNA analysis identifies deep intronic variants causing Alport syndrome and overcomes the problem of negative results of exome sequencing Wang, Xiaoyuan Zhang, Yanqin Ding, Jie Wang, Fang Sci Rep Author Correction Nature Publishing Group UK 2021-11-09 /pmc/articles/PMC8578218/ /pubmed/34754083 http://dx.doi.org/10.1038/s41598-021-01604-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Author Correction Wang, Xiaoyuan Zhang, Yanqin Ding, Jie Wang, Fang Author Correction: mRNA analysis identifies deep intronic variants causing Alport syndrome and overcomes the problem of negative results of exome sequencing |
title | Author Correction: mRNA analysis identifies deep intronic variants causing Alport syndrome and overcomes the problem of negative results of exome sequencing |
title_full | Author Correction: mRNA analysis identifies deep intronic variants causing Alport syndrome and overcomes the problem of negative results of exome sequencing |
title_fullStr | Author Correction: mRNA analysis identifies deep intronic variants causing Alport syndrome and overcomes the problem of negative results of exome sequencing |
title_full_unstemmed | Author Correction: mRNA analysis identifies deep intronic variants causing Alport syndrome and overcomes the problem of negative results of exome sequencing |
title_short | Author Correction: mRNA analysis identifies deep intronic variants causing Alport syndrome and overcomes the problem of negative results of exome sequencing |
title_sort | author correction: mrna analysis identifies deep intronic variants causing alport syndrome and overcomes the problem of negative results of exome sequencing |
topic | Author Correction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8578218/ https://www.ncbi.nlm.nih.gov/pubmed/34754083 http://dx.doi.org/10.1038/s41598-021-01604-9 |
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