Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and Becker muscular dystrophies-Reference-Cited by-同舟云学术

Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and Becker muscular dystrophies

Published:2019-12-03 Issue:3 Volume:41 Page:668-677
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Ling Chao¹^ORCID,Dai Yi²,Fang Li³,Yao Fengxia¹,Liu Zhe¹,Qiu Zhengqing⁴,Cui Liying²,Xia Fan⁵,Zhao Chen⁵,Zhang Shuyang⁶,Wang Kai³⁷,Zhang Xue¹⁸

Affiliation:

1. The Laboratory of Clinical Genetics, Peking Union Medical College Hospital, Chinese Academy of Medical SciencesPeking Union Medical College Beijing China

2. Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical SciencesPeking Union Medical College Beijing China

3. Department of Pathology & Laboratory Medicine, Raymond G. Perelman Center for Cellular and Molecular TherapeuticsThe Children's Hospital of Philadelphia Philadelphia Pennsylvania

4. Department of Pediatrics, Peking Union Medical College Hospital, Chinese Academy of Medical SciencesPeking Union Medical College Beijing China

5. Department of Molecular and Human GeneticsBaylor College of Medicine Houston Texas

6. Department of Cardiology, Peking Union Medical College Hospital, Chinese Academy of Medical SciencesPeking Union Medical College Beijing China

7. Department of Pathology and Laboratory Medicine, Perelman School of MedicineUniversity of Pennsylvania Philadelphia Pennsylvania

8. Institute of Basic Medical Sciences, Chinese Academy of Medical SciencesMcKusick‐Zhang Center for GeneticMedicine, School of Basic Medicine Peking, Union Medical College Beijing China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.23953

Reference37 articles.

1. Aberrant firing of replication origins potentially explains intragenic nonrecurrent rearrangements within genes, including the human DMD gene

2. MEME SUITE: tools for motif discovery and searching

3. PRDM9 Is a Major Determinant of Meiotic Recombination Hotspots in Humans and Mice

4. Meiotic recombination in mammals: localization and regulation

5. The 3D Organization of Chromatin Explains Evolutionary Fragile Genomic Regions

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