Duchenne muscular dystrophy: Genetic and clinical profile in the population of Rajasthan, India

Background: Duchenne Muscular Dystrophy (DMD) is an X-linked recessive muscular dystrophy that affects young boys and is caused by mutation of the dystrophin gene located over X chromosome. Materials and Methods: In this prospective study, 120 clinically diagnosed DMD patients were tested for exon d...

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Detalhes bibliográficos

Principais autores:	Manisha Goyal, Ashok Gupta, Kamlesh Agarwal, Seema Kapoor, Somesh Kumar
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Wolters Kluwer Medknow Publications 2021-01-01
coleção:	Annals of Indian Academy of Neurology
Assuntos:	deletion duchenne muscular dystrophy dystrophin gene muscular dystrophy
Acesso em linha:	http://www.annalsofian.org/article.asp?issn=0972-2327;year=2021;volume=24;issue=6;spage=873;epage=878;aulast=Goyal
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