A different spectrum of DMD gene mutations in local Chinese patients with Duchenne/Becker muscular dystrophy
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference31 articles.
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4. The human dystrophin gene requires 16 hours to be transcribed and is cotranscriptionally spliced
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1. DMD Gene and Dystrophinopathy Phenotypes Associated With Mutations: A Systematic Review for Clinicians;Journal of Clinical Neuromuscular Disease;2023-06
2. Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy;Genes;2023-01-14
3. The position of nonsense mutations can predict the phenotype severity: A survey on the DMD gene;PLOS ONE;2020-08-19
4. Clinical Phenotypes of DMD Exon 51 Skip Equivalent Deletions: A Systematic Review;Journal of Neuromuscular Diseases;2020-06-02
5. Prenatal diagnosis for a Chinese family with a de novo DMD gene mutation;Medicine;2017-12
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