Editorial for the Genetics of Muscular Dystrophies from the Pathogenesis to Gene Therapy Special Issue
Author:
Affiliation:
1. Cardiomyology and Medical Genetics, Department of Experimental Medicine, University of Campania “Luigi Vanvitelli”, 80138 Napoli, Italy
2. IRCCS Fondazione Stella Maris, 56128 Pisa, Italy
Abstract
Funder
Italian Ministry of Health-Ricerca Corrente
Regione Toscana
Publisher
MDPI AG
Subject
Genetics (clinical),Genetics
Link
https://www.mdpi.com/2073-4425/14/4/926/pdf
Reference10 articles.
1. Cotta, A., Souza, L.S., Carvalho, E., Feitosa, L.N., Cunha, A., Navarro, M.M., Valicek, J., Menezes, M.M., Neves, S.V.N., and Xavier-Neto, R. (2022). Central Core Disease: Facial Weakness Differentiating Biallelic from Monoallelic Forms. Genes, 13.
2. Dosi, C., Rubegni, A., Baldacci, J., Galatolo, D., Doccini, S., Astrea, G., Berardinelli, A., Bruno, C., Bruno, G., and Comi, G.P. (2023). Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of RYR1-Related Myopathies. Genes, 14.
3. Viggiano, E., Picillo, E., Passamano, L., Onore, M.E., Piluso, G., Scutifero, M., Torella, A., Nigro, V., and Politano, L. (2023). Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy. Genes, 14.
4. Eser, G., and Topaloğlu, H. (2022). Current Outline of Exon Skipping Trials in Duchenne Muscular Dystrophy. Genes, 13.
5. Park, J., Moon, Y.J., and Kim, D.S. (2023). Miyoshi Muscular Dystrophy Type 1 with Mutated DYSF Gene Misdiagnosed as Becker Muscular Dystrophy: A Case Report and Literature Review. Genes, 14.
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