Original Research
Published on 25 May 2023
Prime editing strategies to mediate exon skipping in DMD gene
in Gene and Cell Therapy
Frontiers in Medicine
doi 10.3389/fmed.2023.1128557
- 8,660 views
- 11 citations
33 articles related to "Dmd Gene"
Articles
Original Research
Published on 03 Sep 2025
Combining PCR to detect junction fragments and deleted exons in the prenatal diagnosis of BMD can effectively identify maternal cell contamination
in Precision Medicine
Frontiers in Medicine
doi 10.3389/fmed.2025.1599498
- 1,186 views
Brief Research Report
Published on 25 Aug 2022
Exonization of a deep intronic long interspersed nuclear element in Becker muscular dystrophy
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2022.979732
- 3,154 views
- 7 citations
Review
Published on 05 Jan 2022
Adeno-Associated Virus (AAV)-Mediated Gene Therapy for Duchenne Muscular Dystrophy: The Issue of Transgene Persistence
in Neuromuscular Disorders and Peripheral Neuropathies
Frontiers in Neurology
doi 10.3389/fneur.2021.814174
- 35,038 views
- 68 citations
Case Report
Published on 10 Mar 2021
Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy
in Neurogenomics
Frontiers in Genetics
doi 10.3389/fgene.2021.605611
- 7,119 views
- 9 citations
Case Report
Published on 27 Sep 2023
A female case report of LGMD2B with compound heterozygous mutations of the DYSF gene and asymptomatic mutation of the X-linked DMD gene
in Neuromuscular Disorders and Peripheral Neuropathies
Frontiers in Neurology
doi 10.3389/fneur.2023.1213090
- 3,614 views
- 1 citation
Original Research
Published on 07 Dec 2021
Combining Protein Expression and Molecular Data Improves Mutation Characterization of Dystrophinopathies
in Neuromuscular Disorders and Peripheral Neuropathies
Frontiers in Neurology
doi 10.3389/fneur.2021.718396
- 5,091 views
- 2 citations
Original Research
Published on 10 Mar 2021
Whole Exome Sequencing Aids the Diagnosis of Fetal Skeletal Dysplasia
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2021.599863
- 6,361 views
- 18 citations
Case Report
Published on 14 Sep 2023
Case report: A rare case of left ventricular noncompaction in two Chinese siblings with becker muscular dystrophy caused by deletion of exons 10 to 12 in the DMD gene
in Cardiovascular Genetics and Systems Medicine
Frontiers in Cardiovascular Medicine
doi 10.3389/fcvm.2023.1243825
- 2,615 views
Original Research
Published on 30 Apr 2021
Sequence and Structure Characteristics of 22 Deletion Breakpoints in Intron 44 of the DMD Gene Based on Long-Read Sequencing
in Genomic Assay Technology
Frontiers in Genetics
doi 10.3389/fgene.2021.638220
- 7,118 views
- 11 citations
Brief Research Report
Published on 26 Nov 2021
Novel Partial Exon 51 Deletion in the Duchenne Muscular Dystrophy Gene Identified via Whole Exome Sequencing and Long-Read Whole-Genome Sequencing
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2021.762987
- 5,439 views
- 8 citations
Review
Published on 28 Mar 2022
Therapeutic Strategies for Dystrophin Replacement in Duchenne Muscular Dystrophy
in Gene and Cell Therapy
Frontiers in Medicine
doi 10.3389/fmed.2022.859930
- 19,915 views
- 37 citations
Case Report
Published on 19 Sep 2023
Case report: a novel deep intronic splice-altering variant in DMD as a cause of Becker muscular dystrophy
in Human and Medical Genomics
Frontiers in Genetics
doi 10.3389/fgene.2023.1226766
- 3,756 views
- 1 citation
Review
Published on 12 May 2020
Advances in Stem Cell Modeling of Dystrophin-Associated Disease: Implications for the Wider World of Dilated Cardiomyopathy
in Striated Muscle Physiology
Frontiers in Physiology
doi 10.3389/fphys.2020.00368
- 7,808 views
- 15 citations
Correction
Published on 15 Jun 2021
Corrigendum: Sequence and Structure Characteristics of 22 Deletion Breakpoints in Intron 44 of the DMD Gene Based on Long-Read Sequencing
in Genomic Assay Technology
Frontiers in Genetics
doi 10.3389/fgene.2021.706540
- 1,869 views
Case Report
Published on 19 Feb 2020
46,XX Testicular Disorders of Sex Development With DMD Gene Mutation: First Case Report Identified Prenatally by Integrated Analyses in China
in Genetics of Common and Rare Diseases
Frontiers in Genetics
doi 10.3389/fgene.2019.01350
- 35,264 views
- 6 citations