Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Editorial
. 2023 Jul 26;14(8):1522.
doi: 10.3390/genes14081522.

Special Issue "Genetics and Epigenetics of Neuromuscular Diseases"

Fabio Coppedè  1
Affiliations
Editorial

Special Issue "Genetics and Epigenetics of Neuromuscular Diseases"

Fabio Coppedè. Genes (Basel). .

Abstract

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

PubMed Disclaimer

Conflict of interest statement

The author declares no conflict of interest.

Similar articles

See all similar articles

Cited by

References

    1. Coppedè F. Epigenetics of neuromuscular disorders. Epigenomics. 2020;12:2125–2139. doi: 10.2217/epi-2020-0282. - DOI - PubMed
    1. Pluta N., Hoffjan S., Zimmer F., Köhler C., Lücke T., Mohr J., Vorgerd M., Nguyen H.H.P., Atlan D., Wolf B., et al. Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular Dystrophy. Genes. 2022;13:1752. doi: 10.3390/genes13101752. - DOI - PMC - PubMed
    1. AlMuhaizea M., Dabbagh O., AlQudairy H., AlHargan A., Alotaibi W., Sami R., AlOtaibi R., Ali M.M., AlHindi H., Colak D., et al. Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population. Genes. 2021;12:1783. doi: 10.3390/genes12111783. - DOI - PMC - PubMed
    1. Serrano-Lorenzo P., Rabasa M., Esteban J., Hidalgo Mayoral I., Domínguez-González C., Blanco-Echevarría A., Garrido-Moraga R., Lucia A., Blázquez A., Rubio J.C., et al. Clinical, Biochemical, and Molecular Characterization of Two Families with Novel Mutations in the LDHA Gene (GSD XI) Genes. 2022;13:1835. doi: 10.3390/genes13101835. - DOI - PMC - PubMed
    1. Jung N.Y., Kwon H.M., Nam D.E., Tamanna N., Lee A.J., Kim S.B., Choi B.-O., Chung K.W. Peripheral Myelin Protein 22 Gene Mutations in Charcot-Marie-Tooth Disease Type 1E Patients. Genes. 2022;13:1219. doi: 10.3390/genes13071219. - DOI - PMC - PubMed

Publication types