Corrigendum: Sequence and Structure Characteristics of 22 Deletion Breakpoints in Intron 44 of the DMD Gene Based on Long-Read Sequencing

Front Genet. 2021 Jun 15:12:706540. doi: 10.3389/fgene.2021.706540. eCollection 2021.

Authors

Chang Geng¹, Yuanren Tong¹, Siwen Zhang², Chao Ling³, Xin Wu², Depeng Wang², Yi Dai¹

Affiliations

¹ Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
² GrandOmics Biosciences, Beijing, China.
³ Laboratory of Clinical Genetics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.

Abstract

[This corrects the article DOI: 10.3389/fgene.2021.638220.].

Keywords: DMD gene; Duchenne and Becker muscular dystrophy; MMEJ; NHEJ; copy number variations; long-read sequencing.

Copyright © 2021 Geng, Tong, Zhang, Ling, Wu, Wang and Dai.

Publication types

Published Erratum