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Special Issue "Genetics and Epigenetics of Neuromuscular Diseases"

Overview
Journal Genes (Basel)
Publisher MDPI
Date 2023 Aug 26
PMID 37628574
Authors
Affiliations
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Abstract

Neuromuscular disorders (NMDs) include several hereditary or acquired conditions that impair the neuromuscular system and muscle function [...].

References
1.
AlMuhaizea M, Dabbagh O, AlQudairy H, AlHargan A, Alotaibi W, Sami R . Phenotypic Variability of Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population. Genes (Basel). 2021; 12(11). PMC: 8620084. DOI: 10.3390/genes12111783. View

2.
Nicoli V, Tabano S, Colapietro P, Maestri M, Ricciardi R, Stoccoro A . Preferential X Chromosome Inactivation as a Mechanism to Explain Female Preponderance in Myasthenia Gravis. Genes (Basel). 2022; 13(4). PMC: 9031138. DOI: 10.3390/genes13040696. View

3.
Pluta N, Hoffjan S, Zimmer F, Kohler C, Lucke T, Mohr J . Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular Dystrophy. Genes (Basel). 2022; 13(10). PMC: 9601614. DOI: 10.3390/genes13101752. View

4.
Lim S, Jung N, Lee A, Choi H, Kwon H, Son W . Genetic and Clinical Studies of Peripheral Neuropathies with Three Small Heat Shock Protein Gene Variants in Korea. Genes (Basel). 2022; 13(3). PMC: 8949397. DOI: 10.3390/genes13030462. View

5.
Coppede F . Epigenetics of neuromuscular disorders. Epigenomics. 2020; 12(23):2125-2139. DOI: 10.2217/epi-2020-0282. View