In-Frame Deletion of Dystrophin Exons 8–50 Results in DMD Phenotype

Mutations that prevent the production of proteins in the DMD gene cause Duchenne muscular dystrophy. Most frequently, these are deletions leading to reading-frame shift. The “reading-frame rule” states that deletions that preserve ORF result in a milder Becker muscular dystrophy. By removing several...

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Detalles Bibliográficos
Autores principales: Egorova, Tatiana V., Galkin, Ivan I., Velyaev, Oleg A., Vassilieva, Svetlana G., Savchenko, Irina M., Loginov, Vyacheslav A., Dzhenkova, Marina A., Korshunova, Diana S., Kozlova, Olga S., Ivankov, Dmitry N., Polikarpova, Anna V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10252864/
https://www.ncbi.nlm.nih.gov/pubmed/37298068
http://dx.doi.org/10.3390/ijms24119117

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10252864/
https://www.ncbi.nlm.nih.gov/pubmed/37298068
http://dx.doi.org/10.3390/ijms24119117

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