Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophy

Abstract Background Duchenne muscular dystrophy (DMD) is the most common muscular dystrophy in the pediatric population. The manifestations of this disease include progressive muscle weakness, gait dysfunction, and motor impairment, leading to a loss of ambulation by the age of 13 years. Molecular d...

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Auteurs principaux:	Gholamreza Zamani, Sareh Hosseinpour, Mahmoud Reza Ashrafi, Mahmoud Mohammadi, Reza Shervin Badv, Ali Reza Tavasoli, Masood Ghahvechi Akbari, Ali Hosseini Bereshneh, Reza Azizi Malamiri, Morteza Heidari
Format:	Artigo
Langue:	Inglês
Publié:	BMC 2022-05-01
Collection:	BMC Neurology
Sujets:	Duchenne muscular dystrophy Phenotype and genetic correlation Iranian patients
Accès en ligne:	https://doi.org/10.1186/s12883-022-02687-1
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