Decoding Neuromuscular Disorders: Insights from Genetics and Epigenetics
A special issue of Genes (ISSN 2073-4425). This special issue belongs to the section "Human Genomics and Genetic Diseases".
Deadline for manuscript submissions: 10 February 2025 | Viewed by 91
Special Issue Editors
Interests: biomarkers; genetics; epigenetics; human diseases; neuromuscular disorders
Special Issue Information
Dear Colleagues,
Neuromuscular disorders (NMDs) encompass a diverse group of conditions affecting patients of different ages and groups. While genetic factors have been extensively studied, emerging evidence highlights the significant role of epigenetics in NMD pathogenesis and treatment. This Special Issue seeks original research articles, reviews, and case reports that advance our understanding of the genetic and epigenetic underpinnings of NMDs. We encourage submissions exploring the complex interplay between genetic variants, epigenetic modifications, and environmental factors in disease development, progression, and treatment. By fostering collaboration among researchers, clinicians, and geneticists, this Special Issue aims to accelerate the development of novel diagnostic tools, therapeutic strategies, and personalized treatment approaches for patients with NMDs.
Dr. Luz Berenice López-Hernández
Dr. Bladimir Roque-Ramírez
Guest Editors
Manuscript Submission Information
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Keywords
- methylation
- microRNAs
- histone modifications
- epigenetics vector development
- genotype/phenotype
- gene expression
- genetic modifiers
- neuromuscular disorders
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