Electrocardiographic Changes in Jordanian Patients With Becker Muscular Dystrophy

Background and aim Becker muscular dystrophy (BMD) is an X-linked disease caused by an in-frame mutation in the dystrophin gene, which is considered an allelic disorder to the most severe form of dystrophinopahies, Duchenne muscular dystrophy, which leads to skeletal and cardiac muscle involvement a...

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Detalles Bibliográficos
Autores principales: Al-Raqad, Mohammed K, Alwahsh, Shorouk, Hejazi, Issa S, Abu-Salah, Osama T, Alshadfan, Lina, Abu-Ledeh, Amal, Ghanem, Nour, Braik, Lana, Raggad, Ahmad D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665640/
https://www.ncbi.nlm.nih.gov/pubmed/38022137
http://dx.doi.org/10.7759/cureus.47553

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665640/
https://www.ncbi.nlm.nih.gov/pubmed/38022137
http://dx.doi.org/10.7759/cureus.47553

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