Next-generation sequencing approach to molecular diagnosis of Iranian patients with Duchenne/Becker muscular dystrophy: Several novel variants identified

Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) constitute the second most prevalent muscular dystrophy, with large deletions or duplications accounting for 66% of cases. No effective treatment exists for DMD/BMD. At present, genetic diagnosis serves as the foundation for gene...

Descripción completa

Detalles Bibliográficos
Autores principales: Bakhshandeh, MohammadKazem, Behroozi, Samira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945705/
https://www.ncbi.nlm.nih.gov/pubmed/36845278
http://dx.doi.org/10.1016/j.ensci.2023.100446

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945705/
https://www.ncbi.nlm.nih.gov/pubmed/36845278
http://dx.doi.org/10.1016/j.ensci.2023.100446

Ejemplares similares