November 20, 2003 article Dystrophin and mutations: one gene, several proteins, multiple phenotypes The Lancet Neurology DOI: 10.1016/s1474-4422(03)00585-4 OpenAlex Authors 0 Author list not loaded yet. Cited by 12 stored of 1,129 Search Sort Most cited Newest Oldest Patent citations Title Any typearticle review book-chapter conference-paper preprint dissertation book dataset other Any fieldAgricultural and Biological Sciences Arts and Humanities Biochemistry, Genetics and Molecular Biology Business, Management and Accounting Chemical Engineering Chemistry Computer Science Decision Sciences Dentistry Earth and Planetary Sciences Economics, Econometrics and Finance Energy Engineering Environmental Science Health Professions Immunology and Microbiology Materials Science Mathematics Medicine Neuroscience Nursing Pharmacology, Toxicology and Pharmaceutics Physics and Astronomy Psychology Social Sciences Veterinary Open access Four new mouse models of Duchenne muscular dystrophy with clinically relevant exon deletions in the human DMD gene 2026 Disease Models & Mechanisms article Biochemistry, Genetics and Molecular Biology Muscle Physiology and Disorders Open access 0 citations Screening cognitive and academic problems in Duchenne Muscular Dystrophy: Validity and reliability of the Kempenhaeghe Learning Questionnaire 2026 Journal of Neuromuscular Diseases article Medicine Neurogenetic and Muscular Disorders Research Open access 0 citations Regional Expression of Dystrophin Gene Transcripts and Proteins in the Mouse Brain 2025 Cells article Biochemistry, Genetics and Molecular Biology Muscle Physiology and Disorders Open access 4 citations Significance of incidental copy number variants in the Duchenne muscular dystrophy gene 2025 Neuromuscular Disorders article Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access 1 citations Dystrophin isoform deficiency and upper‐limb and respiratory function in Duchenne muscular dystrophy 2025 Developmental Medicine & Child Neurology article Biochemistry, Genetics and Molecular Biology Muscle Physiology and Disorders Open access 3 citations Identification of suitable qPCR reference genes for the normalization of gene expression in the BL10-mdx and D2-mdx mouse models of Duchenne muscular dystrophy 2025 PLoS ONE article Biochemistry, Genetics and Molecular Biology Molecular Biology Techniques and Applications Open access 2 citations Genotype and corticosteroid treatment are distinctively associated with gray matter characteristics in patients with Duchenne muscular dystrophy 2024 Neuromuscular Disorders article Biochemistry, Genetics and Molecular Biology Muscle Physiology and Disorders Open access 5 citations Probing diffusion of water and metabolites to assess white matter microstructure in Duchenne muscular dystrophy 2024 NMR in Biomedicine article Medicine Advanced Neuroimaging Techniques and Applications Open access 4 citations T Cell Responses to Dystrophin in a Natural History Study of Duchenne Muscular Dystrophy 2022 Human Gene Therapy article Biochemistry, Genetics and Molecular Biology Muscle Physiology and Disorders Open access 12 citations Integrating Whole-Genome Sequencing in Clinical Genetics: A Novel Disruptive Structural Rearrangement Identified in the Dystrophin Gene (DMD) 2021 International Journal of Molecular Sciences article Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access 12 citations Detailed genetic and functional analysis of the hDMDdel52/mdx mouse model 2020 PLoS ONE article Biochemistry, Genetics and Molecular Biology Muscle Physiology and Disorders Open access cited by 1 patent 30 citations 249th ENMC International Workshop: The role of brain dystrophin in muscular dystrophy: Implications for clinical care and translational research, Hoofddorp, The Netherlands, November 29th–December 1st 2019 2020 Neuromuscular Disorders article Biochemistry, Genetics and Molecular Biology Muscle Physiology and Disorders Open access 32 citations 12 results References 0