Dystrophin muscle enhancer 1 is implicated in the activation of non-muscle isoforms in the skeletal muscle of patients with X-linked dilated cardiomyopathy
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/10/23/2627/9813567/102627.pdf
Cited by 25 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. DMD-Associated Dilated Cardiomyopathy: Genotypes, Phenotypes, and Phenocopies;Circulation: Genomic and Precision Medicine;2023-10
2. Determining the Likelihood of Disease Pathogenicity Among Incidentally Identified Genetic Variants in Rare Dilated Cardiomyopathy‐Associated Genes;Journal of the American Heart Association;2022-10-04
3. Practical approach to the genetic diagnosis of unsolved dystrophinopathies: a stepwise strategy in the genomic era;Journal of Medical Genetics;2020-09-25
4. A novel DMD splicing mutation found in a family responsible for X-linked dilated cardiomyopathy with hyper-CKemia;Medicine;2018-06
5. Transcriptional and epigenetic analyses of the DMD locus reveal novel cis ‑acting DNA elements that govern muscle dystrophin expression;Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms;2017-11
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