The cryptic complex rearrangements involving the DMD gene: etiologic clues about phenotypical differences revealed by optical genome mapping

The cryptic complex rearrangements involving the DMD gene: etiologic clues about phenotypical differences revealed by optical genome mapping

Abstract Background Deletion or duplication in the DMD gene is one of the most common causes of Duchenne and Becker muscular dystrophy (DMD/BMD). However, the pathogenicity of complex rearrangements involving DMD, especially segmental duplications with unknown breakpoints, is not well understood. Th...

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Bibliographic Details
Main Authors: Yunting Ma, Chunrong Gui, Meizhen Shi, Lilin Wei, Junfang He, Bobo Xie, Haiyang Zheng, Xiaoyun Lei, Xianda Wei, Zifeng Cheng, Xu Zhou, Shaoke Chen, Jiefeng Luo, Yan Huang, Baoheng Gui
Format: Article
Language:English
Published: BMC 2024-09-01
Series:Human Genomics
Subjects:
DMD
Complex rearrangement
Breakpoints
Phenotypical differences
Optical genome mapping
Online Access:https://doi.org/10.1186/s40246-024-00653-1

Internet

https://doi.org/10.1186/s40246-024-00653-1

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