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PDFStructural variation
Short report
Likely pathogenic structural variants in genetically unsolved patients with retinitis pigmentosa revealed by long-read sequencing
- Correspondence to Dr Akihiro Fujimoto, Department of Human Genetics, The University of Tokyo, Bunkyo-ku, Tokyo, Japan; afujimoto{at}m.u-tokyo.ac.jp; Dr Masato Akiyama; akiyama.masato.588{at}m.kyushu-u.ac.jp
Citation
Likely pathogenic structural variants in genetically unsolved patients with retinitis pigmentosa revealed by long-read sequencing
Publication history
- Received January 5, 2022
- Accepted May 14, 2022
- First published June 15, 2022.
Online issue publication
May 11, 2023
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- Previous version (9 November 2022).
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© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.